Canonical Allele Identifier: CA1500739595
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144601651A= , CM000666.2:g.144601651A= GRCh38
NC_000004.11:g.145522803A= , CM000666.1:g.145522803A= GRCh37
NC_000004.10:g.145742253A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000649263.1:c.328-185673T= ENSP00000497507.1:n.328-185673T=