HGVS | Genome Assembly |
---|---|
NC_000004.12:g.144601634C>T , CM000666.2:g.144601634C>T | GRCh38 |
NC_000004.11:g.145522786C>T , CM000666.1:g.145522786C>T | GRCh37 |
NC_000004.10:g.145742236C>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000649263.1:c.328-185656G>A | ENSP00000497507.1:n.328-185656G>A |