Canonical Allele Identifier: CA1835374330
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs1821542934

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120212C>T , CM000671.2:g.15120212C>T GRCh38
NC_000009.11:g.15120210C>T , CM000671.1:g.15120210C>T GRCh37
NC_000009.10:g.15110210C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000609203.1:n.549+5518G>A