Canonical Allele Identifier: CA1835374379
Gene: CLCN3P1 HGNC NCBI

Linked Data

dbSNP Id: rs1821543318

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120287C>A , CM000671.2:g.15120287C>A GRCh38
NC_000009.11:g.15120285C>A , CM000671.1:g.15120285C>A GRCh37
NC_000009.10:g.15110285C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609203.1:n.549+5443G>T