Canonical Allele Identifier: CA18006876
Gene: CLCN6 HGNC NCBI
NPPA-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1047561838
MyVariant Identifiers: chr1:g.11903954G>C (hg19) chr1:g.11843897G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11843897G>C , CM000663.2:g.11843897G>C GRCh38
NC_000001.10:g.11903954G>C , CM000663.1:g.11903954G>C GRCh37
NC_000001.9:g.11826541G>C NCBI36
NG_008766.1:g.42748G>C
NG_012926.1:g.8887C>G , LRG_751:g.8887C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000400892.3:c.*1565G>C (CLCN6) ENSP00000496938.1:n.*1565G>C
ENST00000446542.5:n.385G>C (NPPA-AS1)
NR_037806.1:n.1083G>C (NPPA-AS1)
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