Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.38067970C>G , CM000671.2:g.38067970C>G | GRCh38 |
| NC_000009.11:g.38067967C>G , CM000671.1:g.38067967C>G | GRCh37 |
| NC_000009.10:g.38057967C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000377707.4:c.676G>C MANE Select | ENSP00000366936.3:p.Ala226Pro | |
| ENST00000377707.3:c.676G>C | ENSP00000366936.3:p.Ala226Pro | |
| ENST00000540557.1:c.676G>C | ENSP00000457548.1:p.Ala226Pro | |
| NM_003028.2:c.676G>C | NP_003019.2:p.Ala226Pro | |
| NM_003028.3:c.676G>C MANE Select | NP_003019.2:p.Ala226Pro |