Canonical Allele Identifier: CA2783011363
Gene: CLCN3P1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120593A>C , CM000671.2:g.15120593A>C GRCh38
NC_000009.11:g.15120591A>C , CM000671.1:g.15120591A>C GRCh37
NC_000009.10:g.15110591A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609203.1:n.549+5137T>G