Canonical Allele Identifier: CA1108522436
Gene:

Linked Data

dbSNP Id: rs1795950670

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.148560944G>C , CM000669.2:g.148560944G>C GRCh38
NC_000007.13:g.148258036G>C , CM000669.1:g.148258036G>C GRCh37
NC_000007.12:g.147888969G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928099.1:n.300+7156C>G
XR_928100.1:n.433+7156C>G