Linked Data
ClinVar Variation Id:
928
dbSNP Id:
rs28934274
gnomAD v2:
3-33110341-C-T
gnomAD v4:
3-33068849-C-T
PubMed:
PMID:1907800
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.33068849C>T , CM000665.2:g.33068849C>T | GRCh38 |
| NC_000003.11:g.33110341C>T , CM000665.1:g.33110341C>T | GRCh37 |
| NC_000003.10:g.33085345C>T | NCBI36 |
| NG_009005.1:g.33354G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307363.10:c.367G>A MANE Select | ENSP00000306920.4:p.Gly123Arg | |
| ENST00000307363.9:c.367G>A | ENSP00000306920.4:p.Gly123Arg | |
| ENST00000307377.12:c.246-3292G>A | ENSP00000305920.8:n.246-3292G>A | |
| ENST00000399402.7:c.277G>A | ENSP00000382333.2:p.Gly93Arg | |
| ENST00000415454.1:c.76-10580G>A | ENSP00000411813.1:n.76-10580G>A | |
| ENST00000438227.1:c.76-3292G>A | ENSP00000401250.1:n.76-3292G>A | |
| ENST00000440656.1:c.-27G>A | ENSP00000411769.1:n.-27G>A | |
| ENST00000446732.5:c.156-3292G>A | ENSP00000407365.1:n.156-3292G>A | |
| ENST00000450835.1:c.277G>A | ENSP00000403264.1:p.Gly93Arg | |
| ENST00000464355.1:n.325G>A | ||
| ENST00000482097.5:n.109-15300G>A | ||
| ENST00000485698.5:n.137-15300G>A | ||
| ENST00000498537.5:n.133-15300G>A | ||
| NM_000404.2:c.367G>A | NP_000395.2:p.Gly123Arg | |
| NM_000404.3:c.367G>A | NP_000395.2:p.Gly123Arg | |
| NM_001079811.1:c.277G>A | NP_001073279.1:p.Gly93Arg | |
| NM_001079811.2:c.277G>A | NP_001073279.1:p.Gly93Arg | |
| NM_001135602.1:c.246-3292G>A | NP_001129074.1:n.246-3292G>A | |
| NM_001135602.2:c.246-3292G>A | NP_001129074.1:n.246-3292G>A | |
| NM_001317040.1:c.511G>A | NP_001303969.1:p.Gly171Arg | |
| NM_000404.4:c.367G>A MANE Select | NP_000395.3:p.Gly123Arg | |
| NM_001079811.3:c.277G>A | NP_001073279.2:p.Gly93Arg | |
| NM_001135602.3:c.246-3292G>A | NP_001129074.2:n.246-3292G>A | |
| NM_001317040.2:c.511G>A | NP_001303969.2:p.Gly171Arg | |
| NM_001393580.1:c.367G>A | NP_001380509.1:p.Gly123Arg |