HGVS | Genome Assembly |
---|---|
NC_000017.11:g.44375597A>T , CM000679.2:g.44375597A>T | GRCh38 |
NC_000017.10:g.42452965A>T , CM000679.1:g.42452965A>T | GRCh37 |
NC_000017.9:g.39808491A>T | NCBI36 |
NG_008331.1:g.18909T>A , LRG_479:g.18909T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000262407.6:c.2721T>A MANE Select | ENSP00000262407.5:p.Val907= | |
ENST00000648408.1:c.2152T>A | ||
ENST00000262407.5:c.2721T>A | ENSP00000262407.5:p.Val907= | |
ENST00000587295.5:c.253+236T>A | ||
ENST00000592462.5:n.1516T>A | ||
NM_000419.3:c.2721T>A , LRG_479t1:c.2721T>A | NP_000410.2:p.Val907= | |
XM_011524749.1:c.2721T>A | XP_011523051.1:p.Val907= | |
XM_011524750.1:c.2721T>A | XP_011523052.1:p.Val907= | |
NM_000419.4:c.2721T>A | NP_000410.2:p.Val907= | |
NM_000419.5:c.2721T>A MANE Select | NP_000410.2:p.Val907= |