HGVS | Genome Assembly |
---|---|
NC_000009.12:g.2742771T>A , CM000671.2:g.2742771T>A | GRCh38 |
NC_000009.11:g.2742771T>A , CM000671.1:g.2742771T>A | GRCh37 |
NC_000009.10:g.2732771T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000490444.2:c.277-22239A>T | ENSP00000474467.1:n.277-22239A>T |