HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17024018G>T , CM000663.2:g.17024018G>T | GRCh38 |
NC_000001.10:g.17350513G>T , CM000663.1:g.17350513G>T | GRCh37 |
NC_000001.9:g.17223100G>T | NCBI36 |
NG_012340.1:g.35153C>A , LRG_316:g.35153C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000463045.3:c.426C>A | ENSP00000481376.2:p.Tyr142Ter | |
ENST00000491274.6:c.555C>A | ENSP00000480482.2:p.Tyr185Ter | |
ENST00000375499.8:c.597C>A MANE Select | ENSP00000364649.3:p.Tyr199Ter | |
ENST00000375499.7:c.597C>A | ENSP00000364649.3:p.Tyr199Ter | |
ENST00000485515.5:n.531C>A | ||
ENST00000491274.5:c.555C>A | ENSP00000480482.1:p.Tyr185Ter | |
NM_003000.2:c.597C>A , LRG_316t1:c.597C>A | NP_002991.2:p.Tyr199Ter | |
NM_003000.3:c.597C>A MANE Select | NP_002991.2:p.Tyr199Ter |