Canonical Allele Identifier: CA2716183182
Gene:

Linked Data

dbSNP Id: rs2116864841

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.148561039C>T , CM000669.2:g.148561039C>T GRCh38
NC_000007.13:g.148258131C>T , CM000669.1:g.148258131C>T GRCh37
NC_000007.12:g.147889064C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928099.1:n.300+7061G>A
XR_928100.1:n.433+7061G>A