Canonical Allele Identifier: CA191701716

Gene:

Linked Data

• dbSNP Id: rs534965290
• gnomAD v2: 9-25551485-T-C
• gnomAD v3: 9-25551487-T-C
• gnomAD v4: 9-25551487-T-C
• MyVariant Identifiers: chr9:g.25551485T>C (hg19) ; chr9:g.25551487T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.25551487T>C , CM000671.2:g.25551487T>C	GRCh38
NC_000009.11:g.25551485T>C , CM000671.1:g.25551485T>C	GRCh37
NC_000009.10:g.25541485T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_929525.1:n.50-915A>G
XR_929525.2:n.674-915A>G