Canonical Allele Identifier: CA1835374345
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs1821543081

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120243C>A , CM000671.2:g.15120243C>A GRCh38
NC_000009.11:g.15120241C>A , CM000671.1:g.15120241C>A GRCh37
NC_000009.10:g.15110241C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000609203.1:n.549+5487G>T