Canonical Allele Identifier: CA1009280670
Gene:

Linked Data

ClinVar Variation Id: 2734047
ClinVar RCV Id: RCV003527194
dbSNP Id: rs1658038847

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173917430G>C , CM000663.2:g.173917430G>C GRCh38
NC_000001.10:g.173886568G>C , CM000663.1:g.173886568G>C GRCh37
NC_000001.9:g.172153191G>C NCBI36
NG_012462.1:g.4949C>G , LRG_577:g.4949C>G