Linked Data
dbSNP Id:
rs767739170
ExAC:
9:75315490 A / G
gnomAD v2:
9-75315490-A-G
gnomAD v4:
9-72700574-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.72700574A>G , CM000671.2:g.72700574A>G | GRCh38 |
| NC_000009.11:g.75315490A>G , CM000671.1:g.75315490A>G | GRCh37 |
| NC_000009.10:g.74505310A>G | NCBI36 |
| NG_008213.1:g.183774A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297784.10:c.293A>G MANE Select | ENSP00000297784.6:p.Glu98Gly | |
| ENST00000644967.1:c.-77+5860A>G | ENSP00000496159.1:n.-77+5860A>G | |
| ENST00000645053.1:c.-77+5860A>G | ENSP00000493838.1:n.-77+5860A>G | |
| ENST00000645208.2:c.293A>G | ENSP00000494684.1:p.Glu98Gly | |
| ENST00000645773.1:c.236+5860A>G | ENSP00000493698.1:n.236+5860A>G | |
| ENST00000645787.1:n.333A>G | ||
| ENST00000646244.1:n.743A>G | ||
| ENST00000646619.1:c.-77+5860A>G | ENSP00000493726.1:n.-77+5860A>G | |
| ENST00000650689.1:n.660+5860A>G | ||
| ENST00000651183.1:c.-77+5860A>G | ENSP00000498723.1:n.-77+5860A>G | |
| ENST00000297784.9:c.293A>G | ENSP00000297784.5:p.Glu98Gly | |
| ENST00000340019.4:c.293A>G | ENSP00000341433.3:p.Glu98Gly | |
| NM_138691.2:c.293A>G | NP_619636.2:p.Glu98Gly | |
| XM_011518213.1:c.881A>G | XP_011516515.1:p.Glu294Gly | |
| XM_017014256.1:c.296A>G | XP_016869745.1:p.Glu99Gly | |
| NM_138691.3:c.293A>G MANE Select | NP_619636.2:p.Glu98Gly |