Linked Data
ClinVar Variation Id:
165328
dbSNP Id:
rs200405157
ExAC:
X:153641865 C / T
gnomAD v2:
X-153641865-C-T
gnomAD v3:
X-154413528-C-T
gnomAD v4:
X-154413528-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154413528C>T , CM000685.2:g.154413528C>T | GRCh38 |
| NC_000023.10:g.153641865C>T , CM000685.1:g.153641865C>T | GRCh37 |
| NC_000023.9:g.153295059C>T | NCBI36 |
| NG_009634.1:g.6989C>T | |
| NG_012884.2:g.3561G>A | |
| NG_009634.2:g.6994C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698234.1:n.865C>T | ||
| ENST00000698235.1:n.405C>T | ||
| ENST00000698317.1:n.1391C>T | ||
| ENST00000698318.1:n.1264C>T | ||
| ENST00000470127.2:n.609C>T | ||
| ENST00000475699.6:c.385C>T | ENSP00000419854.3:p.His129Tyr | |
| ENST00000476800.2:n.1517C>T | ||
| ENST00000483674.3:n.222C>T | ||
| ENST00000601016.6:c.331C>T MANE Select | ENSP00000469981.1:p.His111Tyr | |
| ENST00000612012.5:c.331C>T | ENSP00000482070.2:p.His111Tyr | |
| ENST00000612460.5:c.331C>T | ENSP00000481037.1:p.His111Tyr | |
| ENST00000614595.2:n.1768C>T | ||
| ENST00000615658.5:n.644C>T | ||
| ENST00000616020.5:c.385C>T | ENSP00000483636.2:p.His129Tyr | |
| ENST00000617701.5:c.*149C>T | ENSP00000481645.1:n.*149C>T | |
| ENST00000621647.2:n.613C>T | ||
| ENST00000652354.1:c.55C>T | ENSP00000498734.1:p.His19Tyr | |
| ENST00000652358.1:c.124C>T | ENSP00000498464.1:p.His42Tyr | |
| ENST00000652390.1:c.250C>T | ENSP00000498858.1:p.His84Tyr | |
| ENST00000652476.1:n.721C>T | ||
| ENST00000652682.1:c.331C>T | ENSP00000498288.1:p.His111Tyr | |
| ENST00000652685.1:n.489C>T | ||
| ENST00000369776.8:c.256C>T | ENSP00000358791.4:p.His86Tyr | |
| ENST00000426231.5:c.247C>T | ||
| ENST00000439735.2:c.331C>T | ENSP00000398193.1:p.His111Tyr | |
| ENST00000475699.5:c.331C>T | ENSP00000419854.2:p.His111Tyr | |
| ENST00000476679.5:n.244C>T | ||
| ENST00000476800.1:n.438C>T | ||
| ENST00000479875.1:n.360C>T | ||
| ENST00000483674.2:n.40C>T | ||
| ENST00000483780.5:n.105C>T | ||
| ENST00000601016.5:c.331C>T | ENSP00000469981.1:p.His111Tyr | |
| ENST00000612012.4:c.385C>T | ENSP00000482070.1:p.His129Tyr | |
| ENST00000612460.4:c.331C>T | ENSP00000481037.1:p.His111Tyr | |
| ENST00000613002.4:c.331C>T | ENSP00000478154.1:p.His111Tyr | |
| ENST00000613634.4:n.651C>T | ||
| ENST00000615658.4:n.744C>T | ||
| ENST00000615986.4:c.*149C>T | ENSP00000480133.1:n.*149C>T | |
| ENST00000616020.4:c.385C>T | ENSP00000483636.1:p.His129Tyr | |
| ENST00000617701.4:c.*161C>T | ENSP00000481645.1:n.*161C>T | |
| ENST00000620808.4:c.*130C>T | ENSP00000479311.1:n.*130C>T | |
| ENST00000621647.1:n.845C>T | ||
| NM_000116.4:c.331C>T | NP_000107.1:p.His111Tyr | |
| NM_001303465.1:c.385C>T | NP_001290394.1:p.His129Tyr | |
| NM_181311.3:c.331C>T | NP_851828.1:p.His111Tyr | |
| NM_181312.3:c.331C>T | NP_851829.1:p.His111Tyr | |
| NM_181313.3:c.331C>T | NP_851830.1:p.His111Tyr | |
| NR_024048.2:n.763C>T | ||
| XM_006724836.1:c.385C>T | XP_006724899.1:p.His129Tyr | |
| XM_006724837.1:c.385C>T | XP_006724900.1:p.His129Tyr | |
| XM_006724839.1:c.385C>T | XP_006724902.1:p.His129Tyr | |
| XM_006724841.2:c.124C>T | XP_006724904.1:p.His42Tyr | |
| XM_006724842.2:c.124C>T | XP_006724905.1:p.His42Tyr | |
| XM_011531189.1:c.385C>T | XP_011529491.1:p.His129Tyr | |
| XM_011531190.1:c.124C>T | XP_011529492.1:p.His42Tyr | |
| XM_011531191.1:c.55C>T | XP_011529493.1:p.His19Tyr | |
| XM_011531192.1:c.52C>T | XP_011529494.1:p.His18Tyr | |
| XR_938511.1:n.688C>T | ||
| XM_006724841.4:c.124C>T | XP_006724904.1:p.His42Tyr | |
| XM_006724842.4:c.124C>T | XP_006724905.1:p.His42Tyr | |
| XM_011531191.2:c.55C>T | XP_011529493.1:p.His19Tyr | |
| XM_017029761.1:c.331C>T | XP_016885250.1:p.His111Tyr | |
| XM_017029762.1:c.385C>T | XP_016885251.1:p.His129Tyr | |
| XM_017029763.1:c.331C>T | XP_016885252.1:p.His111Tyr | |
| XM_017029764.1:c.52C>T | XP_016885253.1:p.His18Tyr | |
| XM_017029765.2:c.124C>T | XP_016885254.1:p.His42Tyr | |
| XM_024452431.1:c.385C>T | XP_024308199.1:p.His129Tyr | |
| NM_000116.5:c.331C>T MANE Select | NP_000107.1:p.His111Tyr | |
| NM_001303465.2:c.385C>T | NP_001290394.1:p.His129Tyr | |
| NM_181311.4:c.331C>T | NP_851828.1:p.His111Tyr | |
| NM_181312.4:c.331C>T | NP_851829.1:p.His111Tyr | |
| NM_181313.4:c.331C>T | NP_851830.1:p.His111Tyr | |
| NR_024048.3:n.742C>T |