HGVS | Genome Assembly |
---|---|
NC_000008.11:g.86739694T>C , CM000670.2:g.86739694T>C | GRCh38 |
NC_000008.10:g.87751922T>C , CM000670.1:g.87751922T>C | GRCh37 |
NC_000008.9:g.87821038T>C | NCBI36 |
NG_016980.1:g.8982A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000320005.6:c.172A>G MANE Select | ENSP00000316605.5:p.Thr58Ala | |
ENST00000681746.1:c.172A>G | ENSP00000505959.1:p.Thr58Ala | |
ENST00000320005.5:c.172A>G | ENSP00000316605.5:p.Thr58Ala | |
ENST00000519777.1:n.154A>G | ||
NM_019098.4:c.172A>G | NP_061971.3:p.Thr58Ala | |
NM_019098.5:c.172A>G MANE Select | NP_061971.3:p.Thr58Ala |