Canonical Allele Identifier: CA1500739645
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144601702T= , CM000666.2:g.144601702T= GRCh38
NC_000004.11:g.145522854T= , CM000666.1:g.145522854T= GRCh37
NC_000004.10:g.145742304T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649263.1:c.328-185724A= ENSP00000497507.1:n.328-185724A=