Canonical Allele Identifier: CA1835374572
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs1006378818

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120442T>C , CM000671.2:g.15120442T>C GRCh38
NC_000009.11:g.15120440T>C , CM000671.1:g.15120440T>C GRCh37
NC_000009.10:g.15110440T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609203.1:n.549+5288A>G