Canonical Allele Identifier: CA416105784
Gene: CLCN6 HGNC NCBI
NPPA-AS1 HGNC NCBI

Linked Data

gnomAD v4: 1-11843772-G-A
MyVariant Identifiers: chr1:g.11903829G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11843772G>A , CM000663.2:g.11843772G>A GRCh38
NC_000001.10:g.11903829G>A , CM000663.1:g.11903829G>A GRCh37
NC_000001.9:g.11826416G>A NCBI36
NG_008766.1:g.42623G>A
NG_012926.1:g.9012C>T , LRG_751:g.9012C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000400892.3:c.*1440G>A (CLCN6) ENSP00000496938.1:n.*1440G>A
ENST00000446542.5:n.260G>A (NPPA-AS1)
NR_037806.1:n.958G>A (NPPA-AS1)