Canonical Allele Identifier: CA191701659

Gene:

Linked Data

• dbSNP Id: rs190270216
• gnomAD v2: 9-25551072-G-T
• gnomAD v3: 9-25551074-G-T
• gnomAD v4: 9-25551074-G-T
• MyVariant Identifiers: chr9:g.25551072G>T (hg19) ; chr9:g.25551074G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.25551074G>T , CM000671.2:g.25551074G>T	GRCh38
NC_000009.11:g.25551072G>T , CM000671.1:g.25551072G>T	GRCh37
NC_000009.10:g.25541072G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_929525.1:n.50-502C>A
XR_929525.2:n.674-502C>A