HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171652028A>G , CM000663.2:g.171652028A>G | GRCh38 |
NC_000001.10:g.171621168A>G , CM000663.1:g.171621168A>G | GRCh37 |
NC_000001.9:g.169887791A>G | NCBI36 |
NG_008859.1:g.5606T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.584T>C MANE Select | ENSP00000037502.5:p.Val195Ala | |
ENST00000638471.1:c.130+454T>C | ENSP00000491206.1:n.130+454T>C | |
ENST00000037502.10:c.584T>C | ENSP00000037502.5:p.Val195Ala | |
ENST00000614688.1:c.584T>C | ENSP00000478680.1:p.Val195Ala | |
NM_000261.1:c.584T>C | NP_000252.1:p.Val195Ala | |
NM_000261.2:c.584T>C MANE Select | NP_000252.1:p.Val195Ala |