HGVS | Genome Assembly |
---|---|
NC_000006.12:g.136822586C>A , CM000668.2:g.136822586C>A | GRCh38 |
NC_000006.11:g.137143724C>A , CM000668.1:g.137143724C>A | GRCh37 |
NC_000006.10:g.137185417C>A | NCBI36 |
NG_008462.1:g.5007C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000541292.6:c.-80C>A | ENSP00000441004.1:n.-80C>A | |
ENST00000318471.4:c.-80C>A | ENSP00000315680.3:n.-80C>A | |
ENST00000367756.8:c.-80C>A | ENSP00000356730.4:n.-80C>A | |
ENST00000541292.5:c.-80C>A | ENSP00000441004.1:n.-80C>A | |
NM_000288.3:c.-80C>A | NP_000279.1:n.-80C>A | |
XM_006715502.1:c.-80C>A | XP_006715565.1:n.-80C>A | |
XM_011535900.1:c.-80C>A | XP_011534202.1:n.-80C>A | |
XM_006715502.2:c.-80C>A | XP_006715565.1:n.-80C>A | |
XM_017010934.2:c.-80C>A | XP_016866423.1:n.-80C>A |