Canonical Allele Identifier: CA1740470136
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.124306385A= , CM000669.2:g.124306385A= GRCh38
NC_000007.13:g.123946439A= , CM000669.1:g.123946439A= GRCh37
NC_000007.12:g.123733675A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002956584.1:n.73-93A=