HGVS | Genome Assembly |
---|---|
NC_000001.11:g.15445715C= , CM000663.2:g.15445715C= | GRCh38 |
NC_000001.10:g.15772210C= , CM000663.1:g.15772210C= | GRCh37 |
NC_000001.9:g.15644797C= | NCBI36 |
NG_009253.1:g.12273C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375949.5:c.758C= MANE Select | ENSP00000365116.4:p.Thr253= | |
ENST00000375943.6:c.*212C= | ENSP00000365110.2:n.*212C= | |
ENST00000375949.4:c.758C= | ENSP00000365116.4:p.Thr253= | |
ENST00000483406.1:n.522C= | ||
NM_007272.2:c.758C= | NP_009203.2:p.Thr253= | |
XM_011540550.1:c.612C= | XP_011538852.1:p.His204= | |
NM_007272.3:c.758C= MANE Select | NP_009203.2:p.Thr253= |