HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17023975G= , CM000663.2:g.17023975G= | GRCh38 |
NC_000001.10:g.17350470G= , CM000663.1:g.17350470G= | GRCh37 |
NC_000001.9:g.17223057G= | NCBI36 |
NG_012340.1:g.35196C= , LRG_316:g.35196C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000463045.3:c.469C= | ENSP00000481376.2:p.Gln157= | |
ENST00000491274.6:c.598C= | ENSP00000480482.2:p.Gln200= | |
ENST00000375499.8:c.640C= MANE Select | ENSP00000364649.3:p.Gln214= | |
ENST00000375499.7:c.640C= | ENSP00000364649.3:p.Gln214= | |
ENST00000485515.5:n.574C= | ||
ENST00000491274.5:c.598C= | ENSP00000480482.1:p.Gln200= | |
NM_003000.2:c.640C= , LRG_316t1:c.640C= | NP_002991.2:p.Gln214= | |
NM_003000.3:c.640C= MANE Select | NP_002991.2:p.Gln214= |