Canonical Allele Identifier: CA861404942

Gene: CLCN3P1

Linked Data

• dbSNP Id: rs1453232500
• MyVariant Identifiers: chr9:g.15120207A>G (hg19) ; chr9:g.15120209A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.15120209A>G , CM000671.2:g.15120209A>G	GRCh38
NC_000009.11:g.15120207A>G , CM000671.1:g.15120207A>G	GRCh37
NC_000009.10:g.15110207A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000609203.1:n.549+5521T>C