Canonical Allele Identifier: CA2783011361
Gene: CLCN3P1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120496G>T , CM000671.2:g.15120496G>T GRCh38
NC_000009.11:g.15120494G>T , CM000671.1:g.15120494G>T GRCh37
NC_000009.10:g.15110494G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609203.1:n.549+5234C>A