Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.8570549T>C , CM000685.2:g.8570549T>C | GRCh38 |
| NC_000023.10:g.8538590T>C , CM000685.1:g.8538590T>C | GRCh37 |
| NC_000023.9:g.8498590T>C | NCBI36 |
| NG_007088.1:g.166638A>G | |
| NG_007088.2:g.166638A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262648.8:c.1012A>G MANE Select | ENSP00000262648.3:p.Ser338Gly | |
| ENST00000262648.7:c.1012A>G | ENSP00000262648.3:p.Ser338Gly | |
| ENST00000488294.1:n.102A>G | ||
| ENST00000619786.1:c.1009A>G | ENSP00000478734.1:p.Ser337Gly | |
| NM_000216.2:c.1012A>G | NP_000207.2:p.Ser338Gly | |
| XM_005274501.3:c.1012A>G | XP_005274558.1:p.Ser338Gly | |
| NM_000216.3:c.1012A>G | NP_000207.2:p.Ser338Gly | |
| XM_005274501.4:c.1012A>G | XP_005274558.1:p.Ser338Gly | |
| NM_000216.4:c.1012A>G MANE Select | NP_000207.2:p.Ser338Gly |