HGVS | Genome Assembly |
---|---|
NC_000004.12:g.4862725C>T , CM000666.2:g.4862725C>T | GRCh38 |
NC_000004.11:g.4864452C>T , CM000666.1:g.4864452C>T | GRCh37 |
NC_000004.10:g.4915353C>T | NCBI36 |
NG_008121.1:g.8061C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382723.5:c.494C>T MANE Select | ENSP00000372170.4:p.Thr165Ile | |
ENST00000382723.4:c.494C>T | ENSP00000372170.4:p.Thr165Ile | |
ENST00000468421.1:n.206C>T | ||
NM_002448.3:c.494C>T MANE Select | NP_002439.2:p.Thr165Ile |