Canonical Allele Identifier: CA1649475251
Gene:

Linked Data

dbSNP Id: rs1772495041

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98048082C>T , CM000668.2:g.98048082C>T GRCh38
NC_000006.11:g.98495958C>T , CM000668.1:g.98495958C>T GRCh37
NC_000006.10:g.98602679C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.372-51104C>T
XR_942809.1:n.372-51104C>T