Canonical Allele Identifier: CA1121649951
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs1821545792
gnomAD v3: 9-15120614-G-A
gnomAD v4: 9-15120614-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120614G>A , CM000671.2:g.15120614G>A GRCh38
NC_000009.11:g.15120612G>A , CM000671.1:g.15120612G>A GRCh37
NC_000009.10:g.15110612G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609203.1:n.549+5116C>T
Search 100 bp 5'
Search 100 bp 3'