Canonical Allele Identifier: CA409015254

Gene: KCNB1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.49374452A>T , CM000682.2:g.49374452A>T	GRCh38
NC_000020.10:g.47990989A>T , CM000682.1:g.47990989A>T	GRCh37
NC_000020.9:g.47424396A>T	NCBI36
NG_041781.1:g.113193T>A
NG_041781.2:g.113193T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004975.4:c.1108T>A MANE Select	NP_004966.1:p.Trp370Arg
ENST00000371741.6:c.1108T>A MANE Select	ENSP00000360806.3:p.Trp370Arg
NM_004975.2:c.1108T>A	NP_004966.1:p.Trp370Arg
NM_004975.3:c.1108T>A	NP_004966.1:p.Trp370Arg
ENST00000371741.5:c.1108T>A	ENSP00000360806.3:p.Trp370Arg
ENST00000635465.1:c.1108T>A	ENSP00000489193.1:p.Trp370Arg
ENST00000635878.1:c.97-75069T>A	ENSP00000489908.1:n.97-75069T>A
ENST00000637341.1:n.206+42428A>T
XM_006723784.2:c.1108T>A	XP_006723847.1:p.Trp370Arg
XM_006723784.3:c.1108T>A	XP_006723847.1:p.Trp370Arg
XM_011528799.1:c.1108T>A	XP_011527101.1:p.Trp370Arg
XM_011528799.2:c.1108T>A	XP_011527101.1:p.Trp370Arg
XR_001754659.1:n.156+42428A>T