Canonical Allele Identifier: CA1121649959

Gene: CLCN3P1

Linked Data

• dbSNP Id: rs1821545958
• gnomAD v3: 9-15120644-A-G
• gnomAD v4: 9-15120644-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.15120644A>G , CM000671.2:g.15120644A>G	GRCh38
NC_000009.11:g.15120642A>G , CM000671.1:g.15120642A>G	GRCh37
NC_000009.10:g.15110642A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609203.1:n.549+5086T>C