Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.66346160C>T , CM000673.2:g.66346160C>T | GRCh38 |
| NC_000011.9:g.66113631C>T , CM000673.1:g.66113631C>T | GRCh37 |
| NC_000011.8:g.65870207C>T | NCBI36 |
| NG_033202.1:g.6531G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006876.3:c.1137G>A MANE Select | NP_006867.1:p.Ala379= |
| ENST00000311181.5:c.1137G>A MANE Select | ENSP00000309096.4:p.Ala379= |
| NM_006876.2:c.1137G>A | NP_006867.1:p.Ala379= |
| ENST00000311181.4:c.1137G>A | ENSP00000309096.4:p.Ala379= |