Canonical Allele Identifier: CA416106190
Gene: CLCN6 HGNC NCBI
NPPA-AS1 HGNC NCBI

Linked Data

gnomAD v4: 1-11843900-C-T
MyVariant Identifiers: chr1:g.11903957C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11843900C>T , CM000663.2:g.11843900C>T GRCh38
NC_000001.10:g.11903957C>T , CM000663.1:g.11903957C>T GRCh37
NC_000001.9:g.11826544C>T NCBI36
NG_008766.1:g.42751C>T
NG_012926.1:g.8884G>A , LRG_751:g.8884G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000400892.3:c.*1568C>T (CLCN6) ENSP00000496938.1:n.*1568C>T
ENST00000446542.5:n.388C>T (NPPA-AS1)
NR_037806.1:n.1086C>T (NPPA-AS1)
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