Canonical Allele Identifier: CA1121649926
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs1821544861
gnomAD v3: 9-15120500-G-A
gnomAD v4: 9-15120500-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120500G>A , CM000671.2:g.15120500G>A GRCh38
NC_000009.11:g.15120498G>A , CM000671.1:g.15120498G>A GRCh37
NC_000009.10:g.15110498G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609203.1:n.549+5230C>T
Search 100 bp 5'
Search 100 bp 3'