HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21200624G>A , CM000674.2:g.21200624G>A | GRCh38 |
NC_000012.11:g.21353558G>A , CM000674.1:g.21353558G>A | GRCh37 |
NC_000012.10:g.21244825G>A | NCBI36 |
NG_011745.1:g.74431G>A , LRG_1022:g.74431G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256958.3:c.1087G>A MANE Select | ENSP00000256958.2:p.Val363Ile | |
ENST00000256958.2:c.1087G>A | ENSP00000256958.2:p.Val363Ile | |
NM_006446.4:c.1087G>A , LRG_1022t1:c.1087G>A | NP_006437.3:p.Val363Ile | |
NM_006446.5:c.1087G>A MANE Select | NP_006437.3:p.Val363Ile |