Canonical Allele Identifier: CA201641753

Gene:

Linked Data

• ClinVar Variation Id: 1266186
• ClinVar RCV Id: RCV001675482
• dbSNP Id: rs10121804
• gnomAD v2: 9-139581983-C-A
• gnomAD v3: 9-136687531-C-A
• gnomAD v4: 9-136687531-C-A
• MyVariant Identifiers: chr9:g.139581983C>A (hg19) ; chr9:g.136687531C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687531C>A , CM000671.2:g.136687531C>A	GRCh38
NC_000009.11:g.139581983C>A , CM000671.1:g.139581983C>A	GRCh37
NC_000009.10:g.138701804C>A	NCBI36
NG_008090.1:g.4929G>T