Canonical Allele Identifier: CA11646920
Gene:
dbSNP:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55547664A>G , CM000666.2:g.55547664A>G GRCh38
NC_000004.11:g.56413831A>G , CM000666.1:g.56413831A>G GRCh37
NC_000004.10:g.56108588A>G NCBI36