Canonical Allele Identifier: CA2778361714
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.148560843A>G , CM000669.2:g.148560843A>G GRCh38
NC_000007.13:g.148257935A>G , CM000669.1:g.148257935A>G GRCh37
NC_000007.12:g.147888868A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928099.1:n.300+7257T>C
XR_928100.1:n.433+7257T>C