HGVS | Genome Assembly |
---|---|
NC_000002.12:g.218881675A= , CM000664.2:g.218881675A= | GRCh38 |
NC_000002.11:g.219746397A= , CM000664.1:g.219746397A= | GRCh37 |
NC_000002.10:g.219454641A= | NCBI36 |
NG_012179.1:g.6143A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000258411.8:c.114-486A= MANE Select | ENSP00000258411.3:n.114-486A= | |
ENST00000258411.7:c.114-486A= | ENSP00000258411.3:n.114-486A= | |
NM_025216.2:c.114-486A= | NP_079492.2:n.114-486A= | |
XM_011511928.1:c.62+208A= | XP_011510230.1:n.62+208A= | |
XM_011511929.1:c.18-486A= | XP_011510231.1:n.18-486A= | |
XM_011511930.1:c.114-486A= | XP_011510232.1:n.114-486A= | |
XM_011511929.2:c.18-486A= | XP_011510231.1:n.18-486A= | |
NM_025216.3:c.114-486A= MANE Select | NP_079492.2:n.114-486A= |