Canonical Allele Identifier: CA11386815
Gene:
ClinVar Variation:
dbSNP:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.171027131T>G , CM000665.2:g.171027131T>G GRCh38
NC_000003.11:g.170744920T>G , CM000665.1:g.170744920T>G GRCh37
NC_000003.10:g.172227614T>G NCBI36
NG_008108.1:g.4849A>C