Canonical Allele Identifier: CA416106555
Gene: CLCN6 HGNC NCBI
NPPA-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.11904084C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11844027C>T , CM000663.2:g.11844027C>T GRCh38
NC_000001.10:g.11904084C>T , CM000663.1:g.11904084C>T GRCh37
NC_000001.9:g.11826671C>T NCBI36
NG_008766.1:g.42878C>T
NG_012926.1:g.8757G>A , LRG_751:g.8757G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1695C>T (CLCN6) ENSP00000496938.1:n.*1695C>T
ENST00000446542.5:n.515C>T (NPPA-AS1)
NR_037806.1:n.1213C>T (NPPA-AS1)