Canonical Allele Identifier: CA73933575
Gene:

Linked Data

ClinVar Variation Id: 3051442
ClinVar RCV Id: RCV004545544
gnomAD v3: 3-48467729-T-C
gnomAD v4: 3-48467729-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48467729T>C , CM000665.2:g.48467729T>C GRCh38
NC_000003.11:g.48509128T>C , CM000665.1:g.48509128T>C GRCh37
NC_000003.10:g.48484132T>C NCBI36
NG_009820.1:g.6900T>C
NG_033100.1:g.38132A>G
NG_009820.2:g.6900T>C