Canonical Allele Identifier: CA1392628846
Gene:

Linked Data

dbSNP Id: rs1708400154

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.109743497A>C , CM000665.2:g.109743497A>C GRCh38
NC_000003.11:g.109462344A>C , CM000665.1:g.109462344A>C GRCh37
NC_000003.10:g.110945034A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924325.1:n.142+63302A>C