Canonical Allele Identifier: CA189418042

Gene: CLCN3P1

Linked Data

• dbSNP Id: rs968091413
• gnomAD v2: 9-15120106-T-C
• gnomAD v3: 9-15120108-T-C
• gnomAD v4: 9-15120108-T-C
• MyVariant Identifiers: chr9:g.15120106T>C (hg19) ; chr9:g.15120108T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.15120108T>C , CM000671.2:g.15120108T>C	GRCh38
NC_000009.11:g.15120106T>C , CM000671.1:g.15120106T>C	GRCh37
NC_000009.10:g.15110106T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000609203.1:n.549+5622A>G