Canonical Allele Identifier: CA416107085
Gene: CLCN6 HGNC NCBI
NPPA-AS1 HGNC NCBI

Linked Data

gnomAD v4: 1-11845660-C-A
MyVariant Identifiers: chr1:g.11905717C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11845660C>A , CM000663.2:g.11845660C>A GRCh38
NC_000001.10:g.11905717C>A , CM000663.1:g.11905717C>A GRCh37
NC_000001.9:g.11828304C>A NCBI36
NG_012926.1:g.7124G>T , LRG_751:g.7124G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000400892.3:c.*1855C>A (CLCN6) ENSP00000496938.1:n.*1855C>A
ENST00000446542.5:n.675C>A (NPPA-AS1)
NR_037806.1:n.1373C>A (NPPA-AS1)