Canonical Allele Identifier: CA1691656456
Gene:

Linked Data

dbSNP Id: rs1803286131

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17957879C>T , CM000669.2:g.17957879C>T GRCh38
NC_000007.13:g.17997502C>T , CM000669.1:g.17997502C>T GRCh37
NC_000007.12:g.17964027C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927078.1:n.271-791C>T