Canonical Allele Identifier: CA652652065
Gene: CLCN3P1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120544G>T , CM000671.2:g.15120544G>T GRCh38
NC_000009.11:g.15120542G>T , CM000671.1:g.15120542G>T GRCh37
NC_000009.10:g.15110542G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000609203.1:n.549+5186C>A