Canonical Allele Identifier: CA249798

Gene:

Linked Data

• ClinVar Variation Id: 132871
• ClinVar RCV Id: RCV000119308
• dbSNP Id: rs4895441
• gnomAD v2: 6-135426573-A-G
• gnomAD v3: 6-135105435-A-G
• gnomAD v4: 6-135105435-A-G
• MyVariant Identifiers: chr6:g.135426573A>G (hg19) ; chr6:g.135105435A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.135105435A>G , CM000668.2:g.135105435A>G	GRCh38
NC_000006.11:g.135426573A>G , CM000668.1:g.135426573A>G	GRCh37
NC_000006.10:g.135468266A>G	NCBI36