Canonical Allele Identifier: CA168906832
Gene:

Linked Data

dbSNP Id: rs908849072

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.148560823G>C , CM000669.2:g.148560823G>C GRCh38
NC_000007.13:g.148257915G>C , CM000669.1:g.148257915G>C GRCh37
NC_000007.12:g.147888848G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928099.1:n.300+7277C>G
XR_928100.1:n.433+7277C>G