Canonical Allele Identifier: CA196910990
Gene:
dbSNP:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.100608250A>G , CM000671.2:g.100608250A>G GRCh38
NC_000009.11:g.103370532A>G , CM000671.1:g.103370532A>G GRCh37
NC_000009.10:g.102410353A>G NCBI36