Linked Data
ClinVar Variation Id:
1668601
ClinVar RCV Id:
RCV002194086
dbSNP Id:
rs758128635
ExAC:
17:44248853 G / A
gnomAD v2:
17-44248853-G-A
gnomAD v4:
17-46171487-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.46171487G>A , CM000679.2:g.46171487G>A | GRCh38 |
| NC_000017.10:g.44248853G>A , CM000679.1:g.44248853G>A | GRCh37 |
| NC_000017.9:g.41604630G>A | NCBI36 |
| NG_032784.1:g.58888C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000432791.7:c.657C>T MANE Select | ENSP00000387393.3:p.His219= | |
| ENST00000571698.2:c.657C>T | ENSP00000459330.2:p.His219= | |
| ENST00000572904.6:c.657C>T | ENSP00000461484.1:p.His219= | |
| ENST00000574590.6:c.657C>T | ENSP00000461812.2:p.His219= | |
| ENST00000574655.6:n.911C>T | ||
| ENST00000575318.6:c.657C>T | ENSP00000461299.1:p.His219= | |
| ENST00000638269.1:n.901C>T | ||
| ENST00000638275.1:c.657C>T | ENSP00000492576.1:p.His219= | |
| ENST00000638902.1:n.761C>T | ||
| ENST00000639099.1:n.907C>T | ||
| ENST00000639150.1:c.23+52184C>T | ENSP00000491906.1:n.23+52184C>T | |
| ENST00000639356.1:n.907C>T | ||
| ENST00000639375.1:n.895C>T | ||
| ENST00000639531.1:c.657C>T | ENSP00000491765.1:p.His219= | |
| ENST00000648792.1:c.657C>T | ENSP00000497628.1:p.His219= | |
| ENST00000262419.10:c.657C>T | ENSP00000262419.6:p.His219= | |
| ENST00000432791.5:c.657C>T | ENSP00000387393.2:p.His219= | |
| ENST00000572904.5:c.657C>T | ENSP00000461484.1:p.His219= | |
| ENST00000574590.5:c.657C>T | ENSP00000461812.1:p.His219= | |
| ENST00000575318.5:c.657C>T | ENSP00000461299.1:p.His219= | |
| NM_001193465.1:c.657C>T | NP_001180394.1:p.His219= | |
| NM_001193466.1:c.657C>T | NP_001180395.1:p.His219= | |
| NM_015443.3:c.657C>T | NP_056258.1:p.His219= | |
| XM_006721823.1:c.657C>T | XP_006721886.1:p.His219= | |
| XM_006721824.2:c.657C>T | XP_006721887.1:p.His219= | |
| XM_011524628.1:c.657C>T | XP_011522930.1:p.His219= | |
| XM_011524629.1:c.657C>T | XP_011522931.1:p.His219= | |
| XM_011524630.1:c.657C>T | XP_011522932.1:p.His219= | |
| XM_011524631.1:c.657C>T | XP_011522933.1:p.His219= | |
| XM_006721823.2:c.657C>T | XP_006721886.1:p.His219= | |
| XM_006721824.4:c.657C>T | XP_006721887.1:p.His219= | |
| XM_011524628.3:c.657C>T | XP_011522930.1:p.His219= | |
| XM_011524629.3:c.657C>T | XP_011522931.1:p.His219= | |
| XM_011524630.3:c.657C>T | XP_011522932.1:p.His219= | |
| XM_011524631.3:c.657C>T | XP_011522933.1:p.His219= | |
| XM_017024488.2:c.657C>T | XP_016879977.1:p.His219= | |
| XM_017024489.1:c.657C>T | XP_016879978.1:p.His219= | |
| NM_001193466.2:c.657C>T | NP_001180395.1:p.His219= | |
| NM_015443.4:c.657C>T MANE Select | NP_056258.1:p.His219= | |
| NM_001193465.2:c.657C>T | NP_001180394.1:p.His219= | |
| NM_001379198.1:c.657C>T | NP_001366127.1:p.His219= |