HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17024018G= , CM000663.2:g.17024018G= | GRCh38 |
NC_000001.10:g.17350513G= , CM000663.1:g.17350513G= | GRCh37 |
NC_000001.9:g.17223100G= | NCBI36 |
NG_012340.1:g.35153C= , LRG_316:g.35153C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000463045.3:c.426C= | ENSP00000481376.2:p.Tyr142= | |
ENST00000491274.6:c.555C= | ENSP00000480482.2:p.Tyr185= | |
ENST00000375499.8:c.597C= MANE Select | ENSP00000364649.3:p.Tyr199= | |
ENST00000375499.7:c.597C= | ENSP00000364649.3:p.Tyr199= | |
ENST00000485515.5:n.531C= | ||
ENST00000491274.5:c.555C= | ENSP00000480482.1:p.Tyr185= | |
NM_003000.2:c.597C= , LRG_316t1:c.597C= | NP_002991.2:p.Tyr199= | |
NM_003000.3:c.597C= MANE Select | NP_002991.2:p.Tyr199= |