Canonical Allele Identifier: CA191701722

Gene:

Linked Data

• dbSNP Id: rs1011104421
• gnomAD v3: 9-25551539-C-G
• gnomAD v4: 9-25551539-C-G
• MyVariant Identifiers: chr9:g.25551537C>G (hg19) ; chr9:g.25551539C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.25551539C>G , CM000671.2:g.25551539C>G	GRCh38
NC_000009.11:g.25551537C>G , CM000671.1:g.25551537C>G	GRCh37
NC_000009.10:g.25541537C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_929525.1:n.50-967G>C
XR_929525.2:n.674-967G>C