Canonical Allele Identifier: CA416106309
Gene: CLCN6 HGNC NCBI
NPPA-AS1 HGNC NCBI

Linked Data

gnomAD v4: 1-11843942-G-T
MyVariant Identifiers: chr1:g.11903999G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11843942G>T , CM000663.2:g.11843942G>T GRCh38
NC_000001.10:g.11903999G>T , CM000663.1:g.11903999G>T GRCh37
NC_000001.9:g.11826586G>T NCBI36
NG_008766.1:g.42793G>T
NG_012926.1:g.8842C>A , LRG_751:g.8842C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1610G>T (CLCN6) ENSP00000496938.1:n.*1610G>T
ENST00000446542.5:n.430G>T (NPPA-AS1)
NR_037806.1:n.1128G>T (NPPA-AS1)