Canonical Allele Identifier: CA2467802765
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.641068T= , CM000686.2:g.641068T= GRCh38
NC_000024.9:g.551803T= , CM000686.1:g.551803T= GRCh37
NC_000024.8:g.521803T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000711141.1:c.614T= ENSP00000518639.1:p.Leu205=
ENST00000711142.1:c.614T= ENSP00000518640.1:p.Leu205=
ENST00000711143.1:c.614T= ENSP00000518641.1:p.Leu205=
ENST00000711145.1:c.614T= ENSP00000518642.1:p.Leu205=