Canonical Allele Identifier: CA862161382

Gene:

Linked Data

• dbSNP Id: rs1190632945
• gnomAD v3: 9-21756123-T-C
• gnomAD v4: 9-21756123-T-C
• MyVariant Identifiers: chr9:g.21756122T>C (hg19) ; chr9:g.21756123T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21756123T>C , CM000671.2:g.21756123T>C	GRCh38
NC_000009.11:g.21756122T>C , CM000671.1:g.21756122T>C	GRCh37
NC_000009.10:g.21746122T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001746563.2:n.163+11702A>G