Canonical Allele Identifier: CA861404944

Gene: CLCN3P1

Linked Data

• dbSNP Id: rs1217075729
• gnomAD v3: 9-15120267-T-C
• gnomAD v4: 9-15120267-T-C
• MyVariant Identifiers: chr9:g.15120265T>C (hg19) ; chr9:g.15120267T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.15120267T>C , CM000671.2:g.15120267T>C	GRCh38
NC_000009.11:g.15120265T>C , CM000671.1:g.15120265T>C	GRCh37
NC_000009.10:g.15110265T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000609203.1:n.549+5463A>G