Canonical Allele Identifier: CA890090313

Gene: CLCNKB

Linked Data

• dbSNP Id: rs1210193678
• MyVariant Identifiers: chr1:g.16374968T>C (hg19) ; chr1:g.16048473T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16048473T>C , CM000663.2:g.16048473T>C	GRCh38
NC_000001.10:g.16374968T>C , CM000663.1:g.16374968T>C	GRCh37
NC_000001.9:g.16247555T>C	NCBI36
NG_013079.1:g.9722T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682338.1:c.577-31T>C	ENSP00000507062.1:n.577-31T>C
ENST00000682793.1:c.577-31T>C	ENSP00000506910.1:n.577-31T>C
ENST00000682838.1:c.*235-31T>C	ENSP00000507652.1:n.*235-31T>C
ENST00000683578.1:c.577-31T>C	ENSP00000507430.1:n.577-31T>C
ENST00000683661.1:n.2112-31T>C
ENST00000684324.1:c.577-31T>C	ENSP00000507937.1:n.577-31T>C
ENST00000684545.1:c.577-31T>C	ENSP00000506733.1:n.577-31T>C
ENST00000684714.1:c.577-31T>C	ENSP00000506861.1:n.577-31T>C
ENST00000684731.1:n.38-31T>C
ENST00000375679.9:c.577-31T>C MANE Select	ENSP00000364831.5:n.577-31T>C
ENST00000375679.8:c.577-31T>C	ENSP00000364831.4:n.577-31T>C
ENST00000619181.4:c.577-31T>C	ENSP00000483866.1:n.577-31T>C
NM_000085.4:c.577-31T>C	NP_000076.2:n.577-31T>C
XM_011540619.1:c.418-31T>C	XP_011538921.1:n.418-31T>C
XM_011540620.1:c.577-31T>C	XP_011538922.1:n.577-31T>C
NM_000085.5:c.577-31T>C MANE Select	NP_000076.2:n.577-31T>C