Canonical Allele Identifier: CA1121649957

Gene: CLCN3P1

Linked Data

• dbSNP Id: rs1821545914
• gnomAD v3: 9-15120626-C-G
• gnomAD v4: 9-15120626-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.15120626C>G , CM000671.2:g.15120626C>G	GRCh38
NC_000009.11:g.15120624C>G , CM000671.1:g.15120624C>G	GRCh37
NC_000009.10:g.15110624C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609203.1:n.549+5104G>C