Canonical Allele Identifier: CA1835374329
Gene: CLCN3P1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120212C= , CM000671.2:g.15120212C= GRCh38
NC_000009.11:g.15120210C= , CM000671.1:g.15120210C= GRCh37
NC_000009.10:g.15110210C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000609203.1:n.549+5518G=