Canonical Allele Identifier: CA190667405

Gene:

Linked Data

• dbSNP Id: rs1015186373
• MyVariant Identifiers: chr9:g.21756061C>T (hg19) ; chr9:g.21756062C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21756062C>T , CM000671.2:g.21756062C>T	GRCh38
NC_000009.11:g.21756061C>T , CM000671.1:g.21756061C>T	GRCh37
NC_000009.10:g.21746061C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001746563.2:n.163+11763G>A