HGVS | Genome Assembly |
---|---|
NC_000020.11:g.45547481A>C , CM000682.2:g.45547481A>C | GRCh38 |
NC_000020.10:g.44176120A>C , CM000682.1:g.44176120A>C | GRCh37 |
NC_000020.9:g.43609534A>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000651288.1:c.-124T>G (EPPIN-WFDC6) | ENSP00000498632.1:n.-124T>G | |
ENST00000409554.1:c.-124T>G (EPPIN) | ENSP00000387153.1:n.-124T>G |