Canonical Allele Identifier: CA1751305284
Gene:

Linked Data

dbSNP Id: rs1795950431

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.148560898C>T , CM000669.2:g.148560898C>T GRCh38
NC_000007.13:g.148257990C>T , CM000669.1:g.148257990C>T GRCh37
NC_000007.12:g.147888923C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928099.1:n.300+7202G>A
XR_928100.1:n.433+7202G>A