HGVS | Genome Assembly |
---|---|
NC_000012.12:g.40197334G>T , CM000674.2:g.40197334G>T | GRCh38 |
NC_000012.11:g.40591136G>T , CM000674.1:g.40591136G>T | GRCh37 |
NC_000012.10:g.38877403G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000416796.5:c.-63+561G>T | ENSP00000398726.1:n.-63+561G>T |