Linked Data
dbSNP Id:
rs774106793
ExAC:
13:113803641 G / A
gnomAD v2:
13-113803641-G-A
gnomAD v3:
13-113149327-G-A
gnomAD v4:
13-113149327-G-A
COSMIC:
COSM4776023
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.113149327G>A , CM000675.2:g.113149327G>A | GRCh38 |
| NC_000013.10:g.113803641G>A , CM000675.1:g.113803641G>A | GRCh37 |
| NC_000013.9:g.112851642G>A | NCBI36 |
| NG_009258.1:g.31529G>A , LRG_548:g.31529G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375559.8:c.1277G>A MANE Select | ENSP00000364709.3:p.Arg426His | |
| ENST00000375551.7:c.*268G>A | ENSP00000364701.3:n.*268G>A | |
| ENST00000375559.7:c.1277G>A | ENSP00000364709.3:p.Arg426His | |
| ENST00000409306.5:c.*268G>A | ENSP00000387092.1:n.*268G>A | |
| NM_000504.3:c.1277G>A , LRG_548t1:c.1277G>A | NP_000495.1:p.Arg426His | |
| NM_001312674.1:c.1145G>A | NP_001299603.1:p.Arg382His | |
| NM_001312675.1:c.*268G>A | NP_001299604.1:n.*268G>A | |
| NM_000504.4:c.1277G>A MANE Select | NP_000495.1:p.Arg426His | |
| NM_001312674.2:c.1145G>A | NP_001299603.1:p.Arg382His | |
| NM_001312675.2:c.*268G>A | NP_001299604.1:n.*268G>A |