Canonical Allele Identifier: CA1500739168
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144601442G= , CM000666.2:g.144601442G= GRCh38
NC_000004.11:g.145522594G= , CM000666.1:g.145522594G= GRCh37
NC_000004.10:g.145742044G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000649263.1:c.328-185464C= ENSP00000497507.1:n.328-185464C=