Linked Data
ClinVar Variation Id:
102481
dbSNP Id:
rs62508582
gnomAD v4:
12-102844370-C-T
ERepo:
CA229288/MONDO:0009861/006
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102844370C>T , CM000674.2:g.102844370C>T | GRCh38 |
| NC_000012.11:g.103238148C>T , CM000674.1:g.103238148C>T | GRCh37 |
| NC_000012.10:g.101762278C>T | NCBI36 |
| NG_008690.1:g.78233G>A | |
| NG_008690.2:g.119041G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553106.6:c.1031G>A MANE Select | ENSP00000448059.1:p.Gly344Asp | |
| ENST00000307000.7:c.1016G>A | ENSP00000303500.2:p.Gly339Asp | |
| ENST00000549247.6:n.790G>A | ||
| ENST00000551114.2:n.693G>A | ||
| ENST00000553106.5:c.1031G>A | ENSP00000448059.1:p.Gly344Asp | |
| ENST00000635477.1:c.135G>A | ||
| ENST00000635528.1:n.546G>A | ||
| NM_000277.1:c.1031G>A | NP_000268.1:p.Gly344Asp | |
| XM_011538422.1:c.974G>A | XP_011536724.1:p.Gly325Asp | |
| NM_000277.2:c.1031G>A | NP_000268.1:p.Gly344Asp | |
| NM_001354304.1:c.1031G>A | NP_001341233.1:p.Gly344Asp | |
| NM_000277.3:c.1031G>A MANE Select | NP_000268.1:p.Gly344Asp | |
| NM_001354304.2:c.1031G>A | NP_001341233.1:p.Gly344Asp |