Canonical Allele Identifier: CA1751305332
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.148560959A= , CM000669.2:g.148560959A= GRCh38
NC_000007.13:g.148258051A= , CM000669.1:g.148258051A= GRCh37
NC_000007.12:g.147888984A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928099.1:n.300+7141T=
XR_928100.1:n.433+7141T=