Canonical Allele Identifier: CA2740077007
Gene: CLCN3P1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15120191T>A , CM000671.2:g.15120191T>A GRCh38
NC_000009.11:g.15120189T>A , CM000671.1:g.15120189T>A GRCh37
NC_000009.10:g.15110189T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000609203.1:n.549+5539A>T