Canonical Allele Identifier: CA201641754

Gene:

Linked Data

• ClinVar Variation Id: 1257569
• ClinVar RCV Id: RCV001668833
• dbSNP Id: rs2385893
• gnomAD v2: 9-139581994-A-C
• gnomAD v3: 9-136687542-A-C
• gnomAD v4: 9-136687542-A-C
• MyVariant Identifiers: chr9:g.139581994A>C (hg19) ; chr9:g.136687542A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687542A>C , CM000671.2:g.136687542A>C	GRCh38
NC_000009.11:g.139581994A>C , CM000671.1:g.139581994A>C	GRCh37
NC_000009.10:g.138701815A>C	NCBI36
NG_008090.1:g.4918T>G