HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240868737G>T , CM000664.2:g.240868737G>T | GRCh38 |
NC_000002.11:g.241808154G>T , CM000664.1:g.241808154G>T | GRCh37 |
NC_000002.10:g.241456827G>T | NCBI36 |
NG_008005.1:g.4993G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307503.3:c.-129G>T | ENSP00000302620.3:n.-129G>T | |
XR_924060.1:n.405+1496C>A |