Canonical Allele Identifier: CA1751305239
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.148560849C= , CM000669.2:g.148560849C= GRCh38
NC_000007.13:g.148257941C= , CM000669.1:g.148257941C= GRCh37
NC_000007.12:g.147888874C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928099.1:n.300+7251G=
XR_928100.1:n.433+7251G=