Canonical Allele Identifier: CA1835374322
Gene: CLCN3P1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120199C= , CM000671.2:g.15120199C= GRCh38
NC_000009.11:g.15120197C= , CM000671.1:g.15120197C= GRCh37
NC_000009.10:g.15110197C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000609203.1:n.549+5531G=