HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240868525T>A , CM000664.2:g.240868525T>A | GRCh38 |
NC_000002.11:g.241807942T>A , CM000664.1:g.241807942T>A | GRCh37 |
NC_000002.10:g.241456615T>A | NCBI36 |
NG_008005.1:g.4781T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307503.3:c.-341T>A | ENSP00000302620.3:n.-341T>A | |
XR_924060.1:n.405+1708A>T |