Linked Data
dbSNP Id:
rs752882820
ExAC:
3:33110339 C / A
gnomAD v2:
3-33110339-C-A
gnomAD v4:
3-33068847-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.33068847C>A , CM000665.2:g.33068847C>A | GRCh38 |
| NC_000003.11:g.33110339C>A , CM000665.1:g.33110339C>A | GRCh37 |
| NC_000003.10:g.33085343C>A | NCBI36 |
| NG_009005.1:g.33356G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307363.10:c.369G>T MANE Select | ENSP00000306920.4:p.Gly123= | |
| ENST00000307363.9:c.369G>T | ENSP00000306920.4:p.Gly123= | |
| ENST00000307377.12:c.246-3290G>T | ENSP00000305920.8:n.246-3290G>T | |
| ENST00000399402.7:c.279G>T | ENSP00000382333.2:p.Gly93= | |
| ENST00000415454.1:c.76-10578G>T | ENSP00000411813.1:n.76-10578G>T | |
| ENST00000438227.1:c.76-3290G>T | ENSP00000401250.1:n.76-3290G>T | |
| ENST00000440656.1:c.-25G>T | ENSP00000411769.1:n.-25G>T | |
| ENST00000446732.5:c.156-3290G>T | ENSP00000407365.1:n.156-3290G>T | |
| ENST00000450835.1:c.279G>T | ENSP00000403264.1:p.Gly93= | |
| ENST00000464355.1:n.327G>T | ||
| ENST00000482097.5:n.109-15298G>T | ||
| ENST00000485698.5:n.137-15298G>T | ||
| ENST00000498537.5:n.133-15298G>T | ||
| NM_000404.2:c.369G>T | NP_000395.2:p.Gly123= | |
| NM_000404.3:c.369G>T | NP_000395.2:p.Gly123= | |
| NM_001079811.1:c.279G>T | NP_001073279.1:p.Gly93= | |
| NM_001079811.2:c.279G>T | NP_001073279.1:p.Gly93= | |
| NM_001135602.1:c.246-3290G>T | NP_001129074.1:n.246-3290G>T | |
| NM_001135602.2:c.246-3290G>T | NP_001129074.1:n.246-3290G>T | |
| NM_001317040.1:c.513G>T | NP_001303969.1:p.Gly171= | |
| NM_000404.4:c.369G>T MANE Select | NP_000395.3:p.Gly123= | |
| NM_001079811.3:c.279G>T | NP_001073279.2:p.Gly93= | |
| NM_001135602.3:c.246-3290G>T | NP_001129074.2:n.246-3290G>T | |
| NM_001317040.2:c.513G>T | NP_001303969.2:p.Gly171= | |
| NM_001393580.1:c.369G>T | NP_001380509.1:p.Gly123= |