Canonical Allele Identifier: CA18006898
Gene: CLCN6 HGNC NCBI
NPPA-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs911842724
MyVariant Identifiers: chr1:g.11904018G>T (hg19) chr1:g.11843961G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11843961G>T , CM000663.2:g.11843961G>T GRCh38
NC_000001.10:g.11904018G>T , CM000663.1:g.11904018G>T GRCh37
NC_000001.9:g.11826605G>T NCBI36
NG_008766.1:g.42812G>T
NG_012926.1:g.8823C>A , LRG_751:g.8823C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000400892.3:c.*1629G>T (CLCN6) ENSP00000496938.1:n.*1629G>T
ENST00000446542.5:n.449G>T (NPPA-AS1)
NR_037806.1:n.1147G>T (NPPA-AS1)
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