Canonical Allele Identifier: CA1500738984
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144601364A= , CM000666.2:g.144601364A= GRCh38
NC_000004.11:g.145522516A= , CM000666.1:g.145522516A= GRCh37
NC_000004.10:g.145741966A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649263.1:c.328-185386T= ENSP00000497507.1:n.328-185386T=