HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67584705G>A , CM000673.2:g.67584705G>A | GRCh38 |
NC_000011.9:g.67352176G>A , CM000673.1:g.67352176G>A | GRCh37 |
NC_000011.8:g.67108752G>A | NCBI36 |
NG_012075.1:g.6111G>A , LRG_723:g.6111G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000398603.6:c.165G>A | ENSP00000381604.1:p.Lys55= | |
ENST00000398606.10:c.165G>A MANE Select | ENSP00000381607.3:p.Lys55= | |
ENST00000646888.1:c.58G>A | ENSP00000494477.1:p.Val20Ile | |
ENST00000398603.5:c.165G>A | ENSP00000381604.1:p.Lys55= | |
ENST00000398606.7:c.165G>A | ENSP00000381607.3:p.Lys55= | |
ENST00000489040.1:n.164G>A | ||
ENST00000494593.1:n.595G>A | ||
ENST00000498765.5:c.128G>A | ||
NM_000852.3:c.165G>A , LRG_723t1:c.165G>A | NP_000843.1:p.Lys55= | |
NM_000852.4:c.165G>A MANE Select | NP_000843.1:p.Lys55= |