Canonical Allele Identifier: CA176707152

Gene:

Linked Data

• dbSNP Id: rs926005609
• gnomAD v2: 8-50024891-T-C
• gnomAD v3: 8-49112332-T-C
• gnomAD v4: 8-49112332-T-C
• MyVariant Identifiers: chr8:g.50024891T>C (hg19) ; chr8:g.49112332T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.49112332T>C , CM000670.2:g.49112332T>C	GRCh38
NC_000008.10:g.50024891T>C , CM000670.1:g.50024891T>C	GRCh37
NC_000008.9:g.50187444T>C	NCBI36