Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.136674736T>G , CM000671.2:g.136674736T>G | GRCh38 |
| NC_000009.11:g.139569188T>G , CM000671.1:g.139569188T>G | GRCh37 |
| NC_000009.10:g.138689009T>G | NCBI36 |
| NG_008090.1:g.17724A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371696.7:c.660A>C MANE Select | ENSP00000360761.2:p.Ser220= | |
| ENST00000371694.7:c.564A>C | ENSP00000360759.3:p.Ser188= | |
| ENST00000371696.6:c.660A>C | ENSP00000360761.2:p.Ser220= | |
| ENST00000472820.1:n.588A>C | ||
| ENST00000538402.1:c.660A>C | ENSP00000438919.1:p.Ser220= | |
| NM_001012727.1:c.564A>C | NP_001012745.1:p.Ser188= | |
| NM_006412.3:c.660A>C | NP_006403.2:p.Ser220= | |
| NM_006412.4:c.660A>C MANE Select | NP_006403.2:p.Ser220= | |
| NM_001012727.2:c.564A>C | NP_001012745.1:p.Ser188= |