Canonical Allele Identifier: CA302917025
Gene:

Linked Data

dbSNP Id: rs1043992198
MyVariant Identifiers: chr18:g.77184948A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.77184948A>G , CM000680.2:g.77184948A>G GRCh38
NC_000018.9:g.74896904A>G , CM000680.1:g.74896904A>G GRCh37
NC_000018.8:g.73025892A>G NCBI36