Canonical Allele Identifier: CA1835374232
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs1821541949

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120122G>C , CM000671.2:g.15120122G>C GRCh38
NC_000009.11:g.15120120G>C , CM000671.1:g.15120120G>C GRCh37
NC_000009.10:g.15110120G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000609203.1:n.549+5608C>G