Linked Data
ClinVar Variation Id:
319684
ClinVar RCV Id:
RCV000266601
dbSNP Id:
rs886052103
COSMIC:
COSM4915703
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.53844186T>A , CM000678.2:g.53844186T>A | GRCh38 |
| NC_000016.9:g.53878098T>A , CM000678.1:g.53878098T>A | GRCh37 |
| NC_000016.8:g.52435599T>A | NCBI36 |
| NG_012969.1:g.145224T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000471389.6:c.783T>A MANE Select | ENSP00000418823.1:p.His261Gln | |
| ENST00000563011.2:c.163T>A | ||
| ENST00000636030.1:n.810T>A | ||
| ENST00000636218.1:c.783T>A | ENSP00000489641.1:p.His261Gln | |
| ENST00000636491.1:c.765T>A | ENSP00000490047.1:p.His255Gln | |
| ENST00000636992.1:c.783T>A | ENSP00000489886.1:p.His261Gln | |
| ENST00000637001.1:c.783T>A | ENSP00000489936.1:p.His261Gln | |
| ENST00000637562.1:c.783T>A | ENSP00000490426.1:p.His261Gln | |
| ENST00000637845.1:c.783T>A | ENSP00000489638.1:p.His261Gln | |
| ENST00000637969.1:c.783T>A | ENSP00000490516.1:p.His261Gln | |
| ENST00000640179.1:c.155T>A | ENSP00000490980.1:p.Ile52Asn | |
| ENST00000464071.1:c.155T>A | ENSP00000418424.1:p.Ile52Asn | |
| ENST00000471389.5:c.783T>A | ENSP00000418823.1:p.His261Gln | |
| NM_001080432.2:c.783T>A | NP_001073901.1:p.His261Gln | |
| XM_011523313.1:c.813T>A | XP_011521615.1:p.His271Gln | |
| XM_011523314.1:c.813T>A | XP_011521616.1:p.His271Gln | |
| XM_011523315.1:c.813T>A | XP_011521617.1:p.His271Gln | |
| XM_011523316.1:c.813T>A | XP_011521618.1:p.His271Gln | |
| NM_001363891.1:c.813T>A | NP_001350820.1:p.His271Gln | |
| NM_001363894.1:c.783T>A | NP_001350823.1:p.His261Gln | |
| NM_001363896.1:c.783T>A | NP_001350825.1:p.His261Gln | |
| NM_001363897.1:c.705T>A | NP_001350826.1:p.His235Gln | |
| NM_001363898.1:c.813T>A | NP_001350827.1:p.His271Gln | |
| NM_001363899.1:c.781+17665T>A | NP_001350828.1:n.781+17665T>A | |
| NM_001363900.1:c.783T>A | NP_001350829.1:p.His261Gln | |
| NM_001363901.1:c.751+17695T>A | NP_001350830.1:n.751+17695T>A | |
| NM_001363903.1:c.783T>A | NP_001350832.1:p.His261Gln | |
| NM_001363905.1:c.270T>A | NP_001350834.1:p.His90Gln | |
| NM_001363988.1:c.783T>A | NP_001350917.1:p.His261Gln | |
| NR_156761.1:n.377T>A | ||
| XM_011523314.3:c.813T>A | XP_011521616.1:p.His271Gln | |
| XM_011523315.3:c.813T>A | XP_011521617.1:p.His271Gln | |
| XM_011523316.3:c.813T>A | XP_011521618.1:p.His271Gln | |
| XM_017023654.2:c.813T>A | XP_016879143.1:p.His271Gln | |
| XM_017023655.2:c.783T>A | XP_016879144.1:p.His261Gln | |
| XM_017023656.2:c.783T>A | XP_016879145.1:p.His261Gln | |
| XM_017023657.2:c.783T>A | XP_016879146.1:p.His261Gln | |
| XM_017023658.2:c.813T>A | XP_016879147.1:p.His271Gln | |
| XM_024450437.1:c.783T>A | XP_024306205.1:p.His261Gln | |
| XR_002957840.1:n.826T>A | ||
| NM_001080432.3:c.783T>A MANE Select | NP_001073901.1:p.His261Gln |