Canonical Allele Identifier: CA416106044
Gene: CLCN6 HGNC NCBI
NPPA-AS1 HGNC NCBI

Linked Data

gnomAD v4: 1-11843851-C-A
MyVariant Identifiers: chr1:g.11903908C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11843851C>A , CM000663.2:g.11843851C>A GRCh38
NC_000001.10:g.11903908C>A , CM000663.1:g.11903908C>A GRCh37
NC_000001.9:g.11826495C>A NCBI36
NG_008766.1:g.42702C>A
NG_012926.1:g.8933G>T , LRG_751:g.8933G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1519C>A (CLCN6) ENSP00000496938.1:n.*1519C>A
ENST00000446542.5:n.339C>A (NPPA-AS1)
NR_037806.1:n.1037C>A (NPPA-AS1)
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