HGVS | Genome Assembly |
---|---|
NC_000017.11:g.44380911C= , CM000679.2:g.44380911C= | GRCh38 |
NC_000017.10:g.42458279C= , CM000679.1:g.42458279C= | GRCh37 |
NC_000017.9:g.39813805C= | NCBI36 |
NG_008331.1:g.13595G= , LRG_479:g.13595G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000262407.6:c.1361G= MANE Select | ENSP00000262407.5:p.Gly454= | |
ENST00000648408.1:c.792G= | ||
ENST00000262407.5:c.1361G= | ENSP00000262407.5:p.Gly454= | |
ENST00000592226.5:n.601G= | ||
ENST00000592462.5:n.156G= | ||
NM_000419.3:c.1361G= , LRG_479t1:c.1361G= | NP_000410.2:p.Gly454= | |
XM_011524749.1:c.1361G= | XP_011523051.1:p.Gly454= | |
XM_011524750.1:c.1361G= | XP_011523052.1:p.Gly454= | |
NM_000419.4:c.1361G= | NP_000410.2:p.Gly454= | |
NM_000419.5:c.1361G= MANE Select | NP_000410.2:p.Gly454= |