Canonical Allele Identifier: CA2716183029
Gene:

Linked Data

dbSNP Id: rs2116864680

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.148560845G>C , CM000669.2:g.148560845G>C GRCh38
NC_000007.13:g.148257937G>C , CM000669.1:g.148257937G>C GRCh37
NC_000007.12:g.147888870G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928099.1:n.300+7255C>G
XR_928100.1:n.433+7255C>G