HGVS | Genome Assembly |
---|---|
NC_000004.12:g.99420771A>G , CM000666.2:g.99420771A>G | GRCh38 |
NC_000004.11:g.100341928A>G , CM000666.1:g.100341928A>G | GRCh37 |
NC_000004.10:g.100560951A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000437033.7:c.587T>C MANE Select | ENSP00000414254.2:p.Val196Ala | |
ENST00000209665.8:c.623T>C | ENSP00000209665.4:p.Val208Ala | |
ENST00000437033.6:c.587T>C | ENSP00000414254.2:p.Val196Ala | |
ENST00000476959.5:c.647T>C | ENSP00000420269.1:p.Val216Ala | |
ENST00000482593.5:c.416T>C | ENSP00000420613.1:p.Val139Ala | |
NM_000673.4:c.623T>C | NP_000664.2:p.Val208Ala | |
NM_001166504.1:c.647T>C | NP_001159976.1:p.Val216Ala | |
NM_000673.7:c.587T>C MANE Select | NP_000664.3:p.Val196Ala | |
NM_001166504.2:c.647T>C | NP_001159976.1:p.Val216Ala |