Canonical Allele Identifier: CA1121649945
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs1321216679
gnomAD v3: 9-15120564-A-G
gnomAD v4: 9-15120564-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120564A>G , CM000671.2:g.15120564A>G GRCh38
NC_000009.11:g.15120562A>G , CM000671.1:g.15120562A>G GRCh37
NC_000009.10:g.15110562A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609203.1:n.549+5166T>C