Canonical Allele Identifier: CA61667999

Gene:

Linked Data

• dbSNP Id: rs1010189883
• gnomAD v2: 2-183685489-T-C
• gnomAD v3: 2-182820762-T-C
• gnomAD v4: 2-182820762-T-C
• MyVariant Identifiers: chr2:g.183685489T>C (hg19) ; chr2:g.182820762T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.182820762T>C , CM000664.2:g.182820762T>C	GRCh38
NC_000002.11:g.183685489T>C , CM000664.1:g.183685489T>C	GRCh37
NC_000002.10:g.183393734T>C	NCBI36