HGVS | Genome Assembly |
---|---|
NC_000013.11:g.52397438A>C , CM000675.2:g.52397438A>C | GRCh38 |
NC_000013.10:g.52971573A>C , CM000675.1:g.52971573A>C | GRCh37 |
NC_000013.9:g.51869574A>C | NCBI36 |
NG_047168.1:g.14057T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000258613.5:c.815T>G MANE Select | ENSP00000258613.4:p.Val272Gly | |
ENST00000648254.1:c.815T>G | ENSP00000497520.1:p.Val272Gly | |
ENST00000258613.4:c.815T>G | ENSP00000258613.4:p.Val272Gly | |
ENST00000349258.8:c.815T>G | ENSP00000340650.4:p.Val272Gly | |
NM_018676.3:c.815T>G | NP_061146.1:p.Val272Gly | |
NM_199263.2:c.815T>G | NP_954872.1:p.Val272Gly | |
NM_018676.4:c.815T>G MANE Select | NP_061146.1:p.Val272Gly | |
NM_199263.3:c.815T>G | NP_954872.1:p.Val272Gly |