Canonical Allele Identifier: CA1835374600

Gene: CLCN3P1

Linked Data

• dbSNP Id: rs1821544689
• gnomAD v3: 9-15120471-G-A
• gnomAD v4: 9-15120471-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.15120471G>A , CM000671.2:g.15120471G>A	GRCh38
NC_000009.11:g.15120469G>A , CM000671.1:g.15120469G>A	GRCh37
NC_000009.10:g.15110469G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609203.1:n.549+5259C>T