Canonical Allele Identifier: CA416106570
Gene: CLCN6 HGNC NCBI
NPPA-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.11904089G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11844032G>T , CM000663.2:g.11844032G>T GRCh38
NC_000001.10:g.11904089G>T , CM000663.1:g.11904089G>T GRCh37
NC_000001.9:g.11826676G>T NCBI36
NG_008766.1:g.42883G>T
NG_012926.1:g.8752C>A , LRG_751:g.8752C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1700G>T (CLCN6) ENSP00000496938.1:n.*1700G>T
ENST00000446542.5:n.520G>T (NPPA-AS1)
NR_037806.1:n.1218G>T (NPPA-AS1)