Canonical Allele Identifier: CA1500739631
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144601679C= , CM000666.2:g.144601679C= GRCh38
NC_000004.11:g.145522831C= , CM000666.1:g.145522831C= GRCh37
NC_000004.10:g.145742281C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649263.1:c.328-185701G= ENSP00000497507.1:n.328-185701G=