Canonical Allele Identifier: CA202098449

Gene:

Linked Data

• dbSNP Id: rs1026695832
• gnomAD v2: 10-4151128-G-C
• gnomAD v3: 10-4108936-G-C
• gnomAD v4: 10-4108936-G-C
• MyVariant Identifiers: chr10:g.4151128G>C (hg19) ; chr10:g.4108936G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.4108936G>C , CM000672.2:g.4108936G>C	GRCh38
NC_000010.10:g.4151128G>C , CM000672.1:g.4151128G>C	GRCh37
NC_000010.9:g.4141128G>C	NCBI36