Linked Data
dbSNP Id:
rs766456667
ExAC:
9:109690642 C / T
gnomAD v2:
9-109690642-C-T
gnomAD v3:
9-106928361-C-T
gnomAD v4:
9-106928361-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.106928361C>T , CM000671.2:g.106928361C>T | GRCh38 |
| NC_000009.11:g.109690642C>T , CM000671.1:g.109690642C>T | GRCh37 |
| NC_000009.10:g.108730463C>T | NCBI36 |
| NG_052913.1:g.70265C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000277225.10:c.4449C>T MANE Select | ENSP00000277225.5:p.His1483= | |
| ENST00000277225.9:c.4449C>T | ENSP00000277225.5:p.His1483= | |
| ENST00000374686.6:c.1098C>T | ENSP00000363818.2:p.His366= | |
| ENST00000441147.6:c.984C>T | ENSP00000397306.2:p.His328= | |
| ENST00000472574.1:c.281-2164C>T | ENSP00000476222.1:n.281-2164C>T | |
| ENST00000480607.5:n.240+1197C>T | ||
| NM_021224.4:c.4449C>T | NP_067047.4:p.His1483= | |
| XM_006717209.2:c.4449C>T | XP_006717272.1:p.His1483= | |
| XM_006717210.2:c.4449C>T | XP_006717273.1:p.His1483= | |
| XM_006717211.2:c.4449C>T | XP_006717274.1:p.His1483= | |
| XM_006717212.2:c.4449C>T | XP_006717275.1:p.His1483= | |
| XM_006717215.2:c.4449C>T | XP_006717278.1:p.His1483= | |
| XM_006717216.2:c.4449C>T | XP_006717279.1:p.His1483= | |
| XM_006717218.2:c.3252+1197C>T | XP_006717281.1:n.3252+1197C>T | |
| XM_011518892.1:c.4449C>T | XP_011517194.1:p.His1483= | |
| NM_001347997.1:c.3252+1197C>T | NP_001334926.1:n.3252+1197C>T | |
| NM_021224.5:c.4449C>T | NP_067047.4:p.His1483= | |
| XM_006717209.4:c.4449C>T | XP_006717272.1:p.His1483= | |
| XM_006717211.4:c.4449C>T | XP_006717274.1:p.His1483= | |
| XM_006717212.4:c.4449C>T | XP_006717275.1:p.His1483= | |
| XM_006717215.4:c.4449C>T | XP_006717278.1:p.His1483= | |
| XM_006717216.4:c.4449C>T | XP_006717279.1:p.His1483= | |
| XM_006717218.4:c.3252+1197C>T | XP_006717281.1:n.3252+1197C>T | |
| XM_017014996.2:c.4449C>T | XP_016870485.1:p.His1483= | |
| XM_017014997.2:c.4449C>T | XP_016870486.1:p.His1483= | |
| XM_017014998.2:c.3252+1197C>T | XP_016870487.1:n.3252+1197C>T | |
| XM_024447629.1:c.4449C>T | XP_024303397.1:p.His1483= | |
| NM_021224.6:c.4449C>T MANE Select | NP_067047.4:p.His1483= | |
| NM_001347997.2:c.3252+1197C>T | NP_001334926.1:n.3252+1197C>T |