Canonical Allele Identifier: CA416106248
Gene: CLCN6 HGNC NCBI
NPPA-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1465924197
gnomAD v2: 1-11903977-G-A
gnomAD v3: 1-11843920-G-A
gnomAD v4: 1-11843920-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11843920G>A , CM000663.2:g.11843920G>A GRCh38
NC_000001.10:g.11903977G>A , CM000663.1:g.11903977G>A GRCh37
NC_000001.9:g.11826564G>A NCBI36
NG_008766.1:g.42771G>A
NG_012926.1:g.8864C>T , LRG_751:g.8864C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000400892.3:c.*1588G>A (CLCN6) ENSP00000496938.1:n.*1588G>A
ENST00000446542.5:n.408G>A (NPPA-AS1)
NR_037806.1:n.1106G>A (NPPA-AS1)