Canonical Allele Identifier: CA890090056

Gene: CLCNKB

Linked Data

• dbSNP Id: rs1222744629
• gnomAD v3: 1-16048186-C-A
• gnomAD v4: 1-16048186-C-A
• MyVariant Identifiers: chr1:g.16374681C>A (hg19) ; chr1:g.16048186C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16048186C>A , CM000663.2:g.16048186C>A	GRCh38
NC_000001.10:g.16374681C>A , CM000663.1:g.16374681C>A	GRCh37
NC_000001.9:g.16247268C>A	NCBI36
NG_013079.1:g.9435C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.498+142C>A	ENSP00000507062.1:n.498+142C>A
ENST00000682793.1:c.498+142C>A	ENSP00000506910.1:n.498+142C>A
ENST00000682838.1:c.*157-157C>A	ENSP00000507652.1:n.*157-157C>A
ENST00000683578.1:c.498+142C>A	ENSP00000507430.1:n.498+142C>A
ENST00000683661.1:n.2033+142C>A
ENST00000684324.1:c.498+142C>A	ENSP00000507937.1:n.498+142C>A
ENST00000684545.1:c.498+142C>A	ENSP00000506733.1:n.498+142C>A
ENST00000684714.1:c.498+142C>A	ENSP00000506861.1:n.498+142C>A
ENST00000375679.9:c.498+142C>A MANE Select	ENSP00000364831.5:n.498+142C>A
ENST00000375679.8:c.498+142C>A	ENSP00000364831.4:n.498+142C>A
ENST00000619181.4:c.498+142C>A	ENSP00000483866.1:n.498+142C>A
NM_000085.4:c.498+142C>A	NP_000076.2:n.498+142C>A
XM_011540619.1:c.339+142C>A	XP_011538921.1:n.339+142C>A
XM_011540620.1:c.498+142C>A	XP_011538922.1:n.498+142C>A
NM_000085.5:c.498+142C>A MANE Select	NP_000076.2:n.498+142C>A