Canonical Allele Identifier: CA1751305228
Gene:

Linked Data

dbSNP Id: rs1795949849

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.148560832G>A , CM000669.2:g.148560832G>A GRCh38
NC_000007.13:g.148257924G>A , CM000669.1:g.148257924G>A GRCh37
NC_000007.12:g.147888857G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928099.1:n.300+7268C>T
XR_928100.1:n.433+7268C>T