HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17022694T= , CM000663.2:g.17022694T= | GRCh38 |
NC_000001.10:g.17349189T= , CM000663.1:g.17349189T= | GRCh37 |
NC_000001.9:g.17221776T= | NCBI36 |
NG_012340.1:g.36477A= , LRG_316:g.36477A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000463045.3:c.508A= | ENSP00000481376.2:p.Thr170= | |
ENST00000491274.6:c.637A= | ENSP00000480482.2:p.Thr213= | |
ENST00000375499.8:c.679A= MANE Select | ENSP00000364649.3:p.Thr227= | |
ENST00000375499.7:c.679A= | ENSP00000364649.3:p.Thr227= | |
ENST00000475049.5:n.104A= | ||
ENST00000485092.5:n.343A= | ||
ENST00000485515.5:n.613A= | ||
NM_003000.2:c.679A= , LRG_316t1:c.679A= | NP_002991.2:p.Thr227= | |
NM_003000.3:c.679A= MANE Select | NP_002991.2:p.Thr227= |