Canonical Allele Identifier: CA1817441807
Gene:

Linked Data

dbSNP Id: rs988167794

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125478456A>C , CM000670.2:g.125478456A>C GRCh38
NC_000008.10:g.126490698A>C , CM000670.1:g.126490698A>C GRCh37
NC_000008.9:g.126559880A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928628.1:n.256+5142A>C