HGVS | Genome Assembly |
---|---|
NC_000022.11:g.32474772G>A , CM000684.2:g.32474772G>A | GRCh38 |
NC_000022.10:g.32870759G>A , CM000684.1:g.32870759G>A | GRCh37 |
NC_000022.9:g.31200759G>A | NCBI36 |
NG_016001.1:g.5053G>A | |
NG_016001.2:g.5053G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266087.11:c.-231G>A | ENSP00000266087.7:n.-231G>A | |
ENST00000420700.5:c.-231G>A | ENSP00000406155.1:n.-231G>A | |
NM_012179.3:c.-231G>A | NP_036311.3:n.-231G>A | |
XM_011530106.1:c.-404G>A | XP_011528408.1:n.-404G>A | |
XM_024452207.1:c.-421G>A | XP_024307975.1:n.-421G>A |