HGVS | Genome Assembly |
---|---|
NC_000022.11:g.32474697T>G , CM000684.2:g.32474697T>G | GRCh38 |
NC_000022.10:g.32870684T>G , CM000684.1:g.32870684T>G | GRCh37 |
NC_000022.9:g.31200684T>G | NCBI36 |
NG_016001.1:g.4978T>G | |
NG_016001.2:g.4978T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266087.11:c.-306T>G | ENSP00000266087.7:n.-306T>G | |
ENST00000420700.5:c.-306T>G | ENSP00000406155.1:n.-306T>G | |
XM_011530106.1:c.-479T>G | XP_011528408.1:n.-479T>G | |
XM_024452207.1:c.-496T>G | XP_024307975.1:n.-496T>G |