Canonical Allele Identifier: CA1835374211
Gene: CLCN3P1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120104T= , CM000671.2:g.15120104T= GRCh38
NC_000009.11:g.15120102T= , CM000671.1:g.15120102T= GRCh37
NC_000009.10:g.15110102T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000609203.1:n.549+5626A=