Canonical Allele Identifier: CA100043896

Gene:

Linked Data

• dbSNP Id: rs191164775
• gnomAD v2: 4-74918712-T-C
• gnomAD v3: 4-74052995-T-C
• gnomAD v4: 4-74052995-T-C
• MyVariant Identifiers: chr4:g.74918712T>C (hg19) ; chr4:g.74052995T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.74052995T>C , CM000666.2:g.74052995T>C	GRCh38
NC_000004.11:g.74918712T>C , CM000666.1:g.74918712T>C	GRCh37
NC_000004.10:g.75137576T>C	NCBI36