Canonical Allele Identifier: CA190667437

Gene:

Linked Data

• dbSNP Id: rs958072572
• MyVariant Identifiers: chr9:g.21756120T>A (hg19) ; chr9:g.21756121T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21756121T>A , CM000671.2:g.21756121T>A	GRCh38
NC_000009.11:g.21756120T>A , CM000671.1:g.21756120T>A	GRCh37
NC_000009.10:g.21746120T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001746563.2:n.163+11704A>T