Canonical Allele Identifier: CA1762561837
Gene:

Linked Data

dbSNP Id: rs1461729

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.9329732A>C , CM000670.2:g.9329732A>C GRCh38
NC_000008.10:g.9187242A>C , CM000670.1:g.9187242A>C GRCh37
NC_000008.9:g.9224652A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040039.1:n.766-2672A>C