Canonical Allele Identifier: CA2368039215

Gene: KCNB1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.49372368A>T , CM000682.2:g.49372368A>T	GRCh38
NC_000020.10:g.47988905A>T , CM000682.1:g.47988905A>T	GRCh37
NC_000020.9:g.47422312A>T	NCBI36
NG_041781.1:g.115277T>A
NG_041781.2:g.115277T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371741.6:c.*615T>A MANE Select	ENSP00000360806.3:n.*615T>A
ENST00000635878.1:c.97-72985T>A	ENSP00000489908.1:n.97-72985T>A
ENST00000636838.1:n.583T>A
ENST00000637131.1:c.736T>A
ENST00000637341.1:n.206+40344A>T
ENST00000371741.5:c.*615T>A	ENSP00000360806.3:n.*615T>A
ENST00000635465.1:c.*615T>A	ENSP00000489193.1:n.*615T>A
NM_004975.2:c.*615T>A	NP_004966.1:n.*615T>A
XM_006723784.2:c.*615T>A	XP_006723847.1:n.*615T>A
XM_011528799.1:c.*615T>A	XP_011527101.1:n.*615T>A
NM_004975.3:c.*615T>A	NP_004966.1:n.*615T>A
XM_006723784.3:c.*615T>A	XP_006723847.1:n.*615T>A
XM_011528799.2:c.*615T>A	XP_011527101.1:n.*615T>A
XR_001754659.1:n.156+40344A>T
NM_004975.4:c.*615T>A MANE Select	NP_004966.1:n.*615T>A