Linked Data
ClinVar Variation Id:
529448
dbSNP Id:
rs139344943
ExAC:
19:13008631 C / T
gnomAD v2:
19-13008631-C-T
gnomAD v3:
19-12897817-C-T
gnomAD v4:
19-12897817-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.12897817C>T , CM000681.2:g.12897817C>T | GRCh38 |
| NC_000019.9:g.13008631C>T , CM000681.1:g.13008631C>T | GRCh37 |
| NC_000019.8:g.12869631C>T | NCBI36 |
| NG_009292.1:g.11658C>T | |
| NG_033049.1:g.26456G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222214.10:c.1197C>T MANE Select | ENSP00000222214.4:p.His399= | |
| ENST00000222214.9:c.1197C>T | ENSP00000222214.4:p.His399= | |
| ENST00000585420.5:n.1527C>T | ||
| ENST00000590472.5:c.241C>T | ||
| ENST00000590530.5:c.*637C>T | ENSP00000468452.1:n.*637C>T | |
| ENST00000591043.1:n.1507C>T | ||
| ENST00000591050.1:c.164C>T | ||
| ENST00000591470.5:c.1197C>T | ENSP00000466845.1:p.His399= | |
| NM_000159.3:c.1197C>T | NP_000150.1:p.His399= | |
| NM_013976.3:c.1197C>T | NP_039663.1:p.His399= | |
| NR_102316.1:n.1360C>T | ||
| NR_102317.1:n.1578C>T | ||
| XM_006722721.2:c.1197C>T | XP_006722784.1:p.His399= | |
| XM_011527899.1:c.1197C>T | XP_011526201.1:p.His399= | |
| XM_011527900.1:c.1197C>T | XP_011526202.1:p.His399= | |
| XM_011527899.2:c.1197C>T | XP_011526201.1:p.His399= | |
| XM_011527900.2:c.1197C>T | XP_011526202.1:p.His399= | |
| XM_017026580.1:c.1197C>T | XP_016882069.1:p.His399= | |
| NM_000159.4:c.1197C>T MANE Select | NP_000150.1:p.His399= | |
| NM_013976.4:c.1197C>T | NP_039663.1:p.His399= | |
| NM_013976.5:c.1197C>T | NP_039663.1:p.His399= |