HGVS | Genome Assembly |
---|---|
NC_000004.12:g.99420555A>C , CM000666.2:g.99420555A>C | GRCh38 |
NC_000004.11:g.100341712A>C , CM000666.1:g.100341712A>C | GRCh37 |
NC_000004.10:g.100560735A>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000437033.7:c.803T>G MANE Select | ENSP00000414254.2:p.Val268Gly | |
ENST00000209665.8:c.839T>G | ENSP00000209665.4:p.Val280Gly | |
ENST00000437033.6:c.803T>G | ENSP00000414254.2:p.Val268Gly | |
ENST00000476959.5:c.863T>G | ENSP00000420269.1:p.Val288Gly | |
ENST00000482593.5:c.632T>G | ENSP00000420613.1:p.Val211Gly | |
NM_000673.4:c.839T>G | NP_000664.2:p.Val280Gly | |
NM_001166504.1:c.863T>G | NP_001159976.1:p.Val288Gly | |
NM_000673.7:c.803T>G MANE Select | NP_000664.3:p.Val268Gly | |
NM_001166504.2:c.863T>G | NP_001159976.1:p.Val288Gly |