Canonical Allele Identifier: CA2561689195
Gene: CLCN3P1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120109G>A , CM000671.2:g.15120109G>A GRCh38
NC_000009.11:g.15120107G>A , CM000671.1:g.15120107G>A GRCh37
NC_000009.10:g.15110107G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000609203.1:n.549+5621C>T