Canonical Allele Identifier: CA185712934
Gene:

Linked Data

ClinVar Variation Id: 979042
ClinVar RCV Id: RCV001257965
dbSNP Id: rs138042437

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127196124A>G , CM000670.2:g.127196124A>G GRCh38
NC_000008.10:g.128208369A>G , CM000670.1:g.128208369A>G GRCh37
NC_000008.9:g.128277551A>G NCBI36