Canonical Allele Identifier: CA1793441478

Gene: KCNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.72866223G= , CM000670.2:g.72866223G=	GRCh38
NC_000008.10:g.73778458G= , CM000670.1:g.73778458G=	GRCh37
NC_000008.9:g.73941012G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000523207.2:c.580-69712G= MANE Select	ENSP00000430846.1:n.580-69712G=
ENST00000523207.1:c.580-69712G=	ENSP00000430846.1:n.580-69712G=
NM_004770.2:c.580-69712G=	NP_004761.2:n.580-69712G=
XM_017013981.1:c.-157+2519G=	XP_016869470.1:n.-157+2519G=
XR_001745620.1:n.1141-69712G=
XR_001745621.1:n.1141-69712G=
NM_004770.3:c.580-69712G= MANE Select	NP_004761.2:n.580-69712G=