Linked Data
ClinVar Variation Id:
1001609
dbSNP Id:
rs553739117
ExAC:
1:201047160 C / T
gnomAD v2:
1-201047160-C-T
gnomAD v3:
1-201078032-C-T
gnomAD v4:
1-201078032-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.201078032C>T , CM000663.2:g.201078032C>T | GRCh38 |
| NC_000001.10:g.201047160C>T , CM000663.1:g.201047160C>T | GRCh37 |
| NC_000001.9:g.199313783C>T | NCBI36 |
| NG_009816.1:g.39535G>A | |
| NG_009816.2:g.39535G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000362061.4:c.1466G>A MANE Select | ENSP00000355192.3:p.Arg489His | |
| ENST00000679417.1:c.*629G>A | ENSP00000506706.1:n.*629G>A | |
| ENST00000680059.1:c.1466G>A | ENSP00000504944.1:p.Arg489His | |
| ENST00000681078.1:c.1466G>A | ENSP00000506645.1:p.Arg489His | |
| ENST00000681190.1:c.1466G>A | ENSP00000506428.1:p.Arg489His | |
| ENST00000681874.1:c.1466G>A | ENSP00000505162.1:p.Arg489His | |
| ENST00000362061.3:c.1466G>A | ENSP00000355192.3:p.Arg489His | |
| ENST00000367338.7:c.1466G>A | ENSP00000356307.3:p.Arg489His | |
| NM_000069.2:c.1466G>A | NP_000060.2:p.Arg489His | |
| XM_005245478.2:c.1466G>A | XP_005245535.1:p.Arg489His | |
| XM_005245478.3:c.1466G>A | XP_005245535.1:p.Arg489His | |
| NM_000069.3:c.1466G>A MANE Select | NP_000060.2:p.Arg489His |