Canonical Allele Identifier: CA416106178
Gene: CLCN6 HGNC NCBI
NPPA-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1645051754
MyVariant Identifiers: chr1:g.11903953T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11843896T>A , CM000663.2:g.11843896T>A GRCh38
NC_000001.10:g.11903953T>A , CM000663.1:g.11903953T>A GRCh37
NC_000001.9:g.11826540T>A NCBI36
NG_008766.1:g.42747T>A
NG_012926.1:g.8888A>T , LRG_751:g.8888A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000400892.3:c.*1564T>A (CLCN6) ENSP00000496938.1:n.*1564T>A
ENST00000446542.5:n.384T>A (NPPA-AS1)
NR_037806.1:n.1082T>A (NPPA-AS1)