Canonical Allele Identifier: CA861404941

Gene: CLCN3P1

Linked Data

• dbSNP Id: rs1199518941
• gnomAD v3: 9-15120206-C-G
• gnomAD v4: 9-15120206-C-G
• MyVariant Identifiers: chr9:g.15120204C>G (hg19) ; chr9:g.15120206C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.15120206C>G , CM000671.2:g.15120206C>G	GRCh38
NC_000009.11:g.15120204C>G , CM000671.1:g.15120204C>G	GRCh37
NC_000009.10:g.15110204C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000609203.1:n.549+5524G>C