Canonical Allele Identifier: CA861404979

Gene: CLCN3P1

Linked Data

• dbSNP Id: rs1321216679
• gnomAD v3: 9-15120564-A-C
• gnomAD v4: 9-15120564-A-C
• MyVariant Identifiers: chr9:g.15120562A>C (hg19) ; chr9:g.15120564A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.15120564A>C , CM000671.2:g.15120564A>C	GRCh38
NC_000009.11:g.15120562A>C , CM000671.1:g.15120562A>C	GRCh37
NC_000009.10:g.15110562A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609203.1:n.549+5166T>G