HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21215495A= , CM000674.2:g.21215495A= | GRCh38 |
NC_000012.11:g.21368429A= , CM000674.1:g.21368429A= | GRCh37 |
NC_000012.10:g.21259696A= | NCBI36 |
NG_011745.1:g.89302A= , LRG_1022:g.89302A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256958.3:c.1498-1624A= MANE Select | ENSP00000256958.2:n.1498-1624A= | |
ENST00000256958.2:c.1498-1624A= | ENSP00000256958.2:n.1498-1624A= | |
NM_006446.4:c.1498-1624A= , LRG_1022t1:c.1498-1624A= | NP_006437.3:n.1498-1624A= | |
NM_006446.5:c.1498-1624A= MANE Select | NP_006437.3:n.1498-1624A= |