Canonical Allele Identifier: CA2718849132
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs1022188498

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120094T>G , CM000671.2:g.15120094T>G GRCh38
NC_000009.11:g.15120092T>G , CM000671.1:g.15120092T>G GRCh37
NC_000009.10:g.15110092T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000609203.1:n.549+5636A>C