Canonical Allele Identifier: CA18006867

Gene: CLCN6 NPPA-AS1

Linked Data

• dbSNP Id: rs975360998
• gnomAD v3: 1-11843843-T-C
• gnomAD v4: 1-11843843-T-C
• MyVariant Identifiers: chr1:g.11903900T>C (hg19) ; chr1:g.11843843T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11843843T>C , CM000663.2:g.11843843T>C	GRCh38
NC_000001.10:g.11903900T>C , CM000663.1:g.11903900T>C	GRCh37
NC_000001.9:g.11826487T>C	NCBI36
NG_008766.1:g.42694T>C
NG_012926.1:g.8941A>G , LRG_751:g.8941A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400892.3:c.*1511T>C (CLCN6)	ENSP00000496938.1:n.*1511T>C
ENST00000446542.5:n.331T>C (NPPA-AS1)
NR_037806.1:n.1029T>C (NPPA-AS1)