Canonical Allele Identifier: CA1121649841

Gene: CLCN3P1

Linked Data

• dbSNP Id: rs1821541918
• gnomAD v3: 9-15120114-A-C
• gnomAD v4: 9-15120114-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.15120114A>C , CM000671.2:g.15120114A>C	GRCh38
NC_000009.11:g.15120112A>C , CM000671.1:g.15120112A>C	GRCh37
NC_000009.10:g.15110112A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000609203.1:n.549+5616T>G