Canonical Allele Identifier: CA191701717

Gene:

Linked Data

• dbSNP Id: rs550792322
• gnomAD v3: 9-25551507-A-C
• gnomAD v4: 9-25551507-A-C
• MyVariant Identifiers: chr9:g.25551505A>C (hg19) ; chr9:g.25551507A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.25551507A>C , CM000671.2:g.25551507A>C	GRCh38
NC_000009.11:g.25551505A>C , CM000671.1:g.25551505A>C	GRCh37
NC_000009.10:g.25541505A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_929525.1:n.50-935T>G
XR_929525.2:n.674-935T>G