Canonical Allele Identifier: CA89826665
Gene:

Linked Data

dbSNP Id: rs1028883036
MyVariant Identifiers: chr3:g.185826380G>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.185826380G>C , CM000665.2:g.185826380G>C GRCh38
NC_000003.11:g.185544168G>C , CM000665.1:g.185544168G>C GRCh37
NC_000003.10:g.187026862G>C NCBI36
NG_011602.1:g.3660C>G