Canonical Allele Identifier: CA1835374210
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs1821541794

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120102T>A , CM000671.2:g.15120102T>A GRCh38
NC_000009.11:g.15120100T>A , CM000671.1:g.15120100T>A GRCh37
NC_000009.10:g.15110100T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000609203.1:n.549+5628A>T