Canonical Allele Identifier: CA2513468859
Gene: CLCN3P1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120447A>T , CM000671.2:g.15120447A>T GRCh38
NC_000009.11:g.15120445A>T , CM000671.1:g.15120445A>T GRCh37
NC_000009.10:g.15110445A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609203.1:n.549+5283T>A