HGVS | Genome Assembly |
---|---|
NC_000021.9:g.31667310G>A , CM000683.2:g.31667310G>A | GRCh38 |
NC_000021.8:g.33039623G>A , CM000683.1:g.33039623G>A | GRCh37 |
NC_000021.7:g.31961494G>A | NCBI36 |
NG_008689.1:g.12689G>A , LRG_652:g.12689G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270142.11:c.292G>A MANE Select | ENSP00000270142.7:p.Val98Met | |
ENST00000270142.10:c.292G>A | ENSP00000270142.6:p.Val98Met | |
ENST00000389995.4:c.235G>A | ENSP00000374645.4:p.Val79Met | |
ENST00000470944.1:n.1220G>A | ||
ENST00000476106.5:n.555G>A | ||
NM_000454.4:c.292G>A , LRG_652t1:c.292G>A | NP_000445.1:p.Val98Met | |
NM_000454.5:c.292G>A MANE Select | NP_000445.1:p.Val98Met |