Canonical Allele Identifier: CA1762557073
Gene:

Linked Data

dbSNP Id: rs9987289

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.9325848A>C , CM000670.2:g.9325848A>C GRCh38
NC_000008.10:g.9183358A>C , CM000670.1:g.9183358A>C GRCh37
NC_000008.9:g.9220768A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040039.1:n.364-54A>C