Canonical Allele Identifier: CA1121649905

Gene: CLCN3P1

Linked Data

• dbSNP Id: rs1821544121
• gnomAD v3: 9-15120393-C-T
• gnomAD v4: 9-15120393-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.15120393C>T , CM000671.2:g.15120393C>T	GRCh38
NC_000009.11:g.15120391C>T , CM000671.1:g.15120391C>T	GRCh37
NC_000009.10:g.15110391C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609203.1:n.549+5337G>A