Canonical Allele Identifier: CA1121649933
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs1821545166
gnomAD v3: 9-15120530-G-A
gnomAD v4: 9-15120530-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120530G>A , CM000671.2:g.15120530G>A GRCh38
NC_000009.11:g.15120528G>A , CM000671.1:g.15120528G>A GRCh37
NC_000009.10:g.15110528G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609203.1:n.549+5200C>T
Search 100 bp 5'
Search 100 bp 3'