HGVS | Genome Assembly |
---|---|
NC_000002.12:g.27085170G>A , CM000664.2:g.27085170G>A | GRCh38 |
NC_000002.11:g.27308038G>A , CM000664.1:g.27308038G>A | GRCh37 |
NC_000002.10:g.27161542G>A | NCBI36 |
NG_012199.1:g.3428G>A | |
NG_046849.1:g.11604G>A | |
NG_012199.2:g.3428G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000380320.9:c.2586G>A MANE Select | ENSP00000369677.4:p.Gly862= | |
ENST00000380320.8:c.2586G>A | ENSP00000369677.4:p.Gly862= | |
ENST00000433140.1:c.578G>A | ||
NM_007046.3:c.2586G>A | NP_008977.1:p.Gly862= | |
XM_006711928.2:c.2575+162G>A | XP_006711991.1:n.2575+162G>A | |
NM_007046.4:c.2586G>A MANE Select | NP_008977.1:p.Gly862= |