Canonical Allele Identifier: CA189418102

Gene: CLCN3P1

Linked Data

• dbSNP Id: rs764057880
• MyVariant Identifiers: chr9:g.15120264C>G (hg19) ; chr9:g.15120266C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.15120266C>G , CM000671.2:g.15120266C>G	GRCh38
NC_000009.11:g.15120264C>G , CM000671.1:g.15120264C>G	GRCh37
NC_000009.10:g.15110264C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000609203.1:n.549+5464G>C