Canonical Allele Identifier: CA416107110
Gene: CLCN6 HGNC NCBI
NPPA-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1645062994
gnomAD v3: 1-11845669-T-C
gnomAD v4: 1-11845669-T-C
MyVariant Identifiers: chr1:g.11905726T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11845669T>C , CM000663.2:g.11845669T>C GRCh38
NC_000001.10:g.11905726T>C , CM000663.1:g.11905726T>C GRCh37
NC_000001.9:g.11828313T>C NCBI36
NG_012926.1:g.7115A>G , LRG_751:g.7115A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000400892.3:c.*1864T>C (CLCN6) ENSP00000496938.1:n.*1864T>C
ENST00000446542.5:n.684T>C (NPPA-AS1)
NR_037806.1:n.1382T>C (NPPA-AS1)