Canonical Allele Identifier: CA11014478
Gene:
dbSNP:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.59093319C>G , CM000664.2:g.59093319C>G GRCh38
NC_000002.11:g.59320454C>G , CM000664.1:g.59320454C>G GRCh37
NC_000002.10:g.59173958C>G NCBI36