Canonical Allele Identifier: CA190667322

Gene:

Linked Data

• dbSNP Id: rs1045538091
• gnomAD v3: 9-21755991-C-G
• gnomAD v4: 9-21755991-C-G
• MyVariant Identifiers: chr9:g.21755990C>G (hg19) ; chr9:g.21755991C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.21755991C>G , CM000671.2:g.21755991C>G	GRCh38
NC_000009.11:g.21755990C>G , CM000671.1:g.21755990C>G	GRCh37
NC_000009.10:g.21745990C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001746563.2:n.163+11834G>C