HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17022652A= , CM000663.2:g.17022652A= | GRCh38 |
NC_000001.10:g.17349147A= , CM000663.1:g.17349147A= | GRCh37 |
NC_000001.9:g.17221734A= | NCBI36 |
NG_012340.1:g.36519T= , LRG_316:g.36519T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000463045.3:c.550T= | ENSP00000481376.2:p.Tyr184= | |
ENST00000491274.6:c.679T= | ENSP00000480482.2:p.Tyr227= | |
ENST00000375499.8:c.721T= MANE Select | ENSP00000364649.3:p.Tyr241= | |
ENST00000375499.7:c.721T= | ENSP00000364649.3:p.Tyr241= | |
ENST00000475049.5:n.146T= | ||
ENST00000485092.5:n.385T= | ||
ENST00000485515.5:n.655T= | ||
NM_003000.2:c.721T= , LRG_316t1:c.721T= | NP_002991.2:p.Tyr241= | |
NM_003000.3:c.721T= MANE Select | NP_002991.2:p.Tyr241= |