Canonical Allele Identifier: CA2716183028
Gene:

Linked Data

dbSNP Id: rs2116864673

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.148560829G>T , CM000669.2:g.148560829G>T GRCh38
NC_000007.13:g.148257921G>T , CM000669.1:g.148257921G>T GRCh37
NC_000007.12:g.147888854G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928099.1:n.300+7271C>A
XR_928100.1:n.433+7271C>A