Linked Data
dbSNP Id:
rs199475675
ExAC:
12:103246634 C / A
gnomAD v2:
12-103246634-C-A
gnomAD v4:
12-102852856-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102852856C>A , CM000674.2:g.102852856C>A | GRCh38 |
| NC_000012.11:g.103246634C>A , CM000674.1:g.103246634C>A | GRCh37 |
| NC_000012.10:g.101770764C>A | NCBI36 |
| NG_008690.1:g.69747G>T | |
| NG_008690.2:g.110555G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553106.6:c.801G>T MANE Select | ENSP00000448059.1:p.Gln267His | |
| ENST00000307000.7:c.786G>T | ENSP00000303500.2:p.Gln262His | |
| ENST00000549247.6:n.560G>T | ||
| ENST00000553106.5:c.801G>T | ENSP00000448059.1:p.Gln267His | |
| NM_000277.1:c.801G>T | NP_000268.1:p.Gln267His | |
| XM_011538422.1:c.801G>T | XP_011536724.1:p.Gln267His | |
| NM_000277.2:c.801G>T | NP_000268.1:p.Gln267His | |
| NM_001354304.1:c.801G>T | NP_001341233.1:p.Gln267His | |
| NM_000277.3:c.801G>T MANE Select | NP_000268.1:p.Gln267His | |
| NM_001354304.2:c.801G>T | NP_001341233.1:p.Gln267His |