HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17022719C= , CM000663.2:g.17022719C= | GRCh38 |
NC_000001.10:g.17349214C= , CM000663.1:g.17349214C= | GRCh37 |
NC_000001.9:g.17221801C= | NCBI36 |
NG_012340.1:g.36452G= , LRG_316:g.36452G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000463045.3:c.483G= | ENSP00000481376.2:p.Trp161= | |
ENST00000491274.6:c.612G= | ENSP00000480482.2:p.Trp204= | |
ENST00000375499.8:c.654G= MANE Select | ENSP00000364649.3:p.Trp218= | |
ENST00000375499.7:c.654G= | ENSP00000364649.3:p.Trp218= | |
ENST00000475049.5:n.79G= | ||
ENST00000485092.5:n.318G= | ||
ENST00000485515.5:n.588G= | ||
NM_003000.2:c.654G= , LRG_316t1:c.654G= | NP_002991.2:p.Trp218= | |
NM_003000.3:c.654G= MANE Select | NP_002991.2:p.Trp218= |