Canonical Allele Identifier: CA1835374229
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs1821541939

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120119C>G , CM000671.2:g.15120119C>G GRCh38
NC_000009.11:g.15120117C>G , CM000671.1:g.15120117C>G GRCh37
NC_000009.10:g.15110117C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000609203.1:n.549+5611G>C