Canonical Allele Identifier: CA14854097

Gene: KCNB1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.49394471G>A , CM000682.2:g.49394471G>A	GRCh38
NC_000020.10:g.48011008G>A , CM000682.1:g.48011008G>A	GRCh37
NC_000020.9:g.47444415G>A	NCBI36
NG_041781.1:g.93174C>T
NG_041781.2:g.93174C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371741.6:c.568-19479C>T MANE Select	ENSP00000360806.3:n.568-19479C>T
ENST00000635878.1:c.96+87443C>T	ENSP00000489908.1:n.96+87443C>T
ENST00000637341.1:n.207-28621G>A
ENST00000371741.5:c.568-19479C>T	ENSP00000360806.3:n.568-19479C>T
ENST00000635465.1:c.568-19479C>T	ENSP00000489193.1:n.568-19479C>T
NM_004975.2:c.568-19479C>T	NP_004966.1:n.568-19479C>T
XM_006723784.2:c.568-19479C>T	XP_006723847.1:n.568-19479C>T
XM_011528799.1:c.568-19479C>T	XP_011527101.1:n.568-19479C>T
NM_004975.3:c.568-19479C>T	NP_004966.1:n.568-19479C>T
XM_006723784.3:c.568-19479C>T	XP_006723847.1:n.568-19479C>T
XM_011528799.2:c.568-19479C>T	XP_011527101.1:n.568-19479C>T
XR_001754659.1:n.157-32181G>A
NM_004975.4:c.568-19479C>T MANE Select	NP_004966.1:n.568-19479C>T