Canonical Allele Identifier: CA1121649950
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs1821545731
gnomAD v3: 9-15120602-A-G
gnomAD v4: 9-15120602-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120602A>G , CM000671.2:g.15120602A>G GRCh38
NC_000009.11:g.15120600A>G , CM000671.1:g.15120600A>G GRCh37
NC_000009.10:g.15110600A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609203.1:n.549+5128T>C