Canonical Allele Identifier: CA1704517782
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.46032961C= , CM000669.2:g.46032961C= GRCh38
NC_000007.13:g.46072559C= , CM000669.1:g.46072559C= GRCh37
NC_000007.12:g.46039084C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745203.1:n.1270-3657C=