Canonical Allele Identifier: CA2718932280
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs2118116932

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120537G>C , CM000671.2:g.15120537G>C GRCh38
NC_000009.11:g.15120535G>C , CM000671.1:g.15120535G>C GRCh37
NC_000009.10:g.15110535G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609203.1:n.549+5193C>G