HGVS | Genome Assembly |
---|---|
NC_000006.12:g.44313395G>A , CM000668.2:g.44313395G>A | GRCh38 |
NC_000006.11:g.44281132G>A , CM000668.1:g.44281132G>A | GRCh37 |
NC_000006.10:g.44389110G>A | NCBI36 |
NG_031952.1:g.4932C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000505802.1:c.855+5753G>A | ||
NM_001318876.2:c.946-128495G>A | NP_001305805.1:n.946-128495G>A |