Canonical Allele Identifier: CA1751305286
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.148560905T= , CM000669.2:g.148560905T= GRCh38
NC_000007.13:g.148257997T= , CM000669.1:g.148257997T= GRCh37
NC_000007.12:g.147888930T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928099.1:n.300+7195A=
XR_928100.1:n.433+7195A=