Canonical Allele Identifier: CA1069061812
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144601407A>G , CM000666.2:g.144601407A>G GRCh38
NC_000004.11:g.145522559A>G , CM000666.1:g.145522559A>G GRCh37
NC_000004.10:g.145742009A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649263.1:c.328-185429T>C ENSP00000497507.1:n.328-185429T>C