Canonical Allele Identifier: CA1793441503

Gene: KCNB2

Linked Data

• dbSNP Id: rs1805516607

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.72866272dup , CM000670.2:g.72866272dup	GRCh38
NC_000008.10:g.73778507dup , CM000670.1:g.73778507dup	GRCh37
NC_000008.9:g.73941061dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000523207.2:c.580-69663dup MANE Select	ENSP00000430846.1:n.580-69663dup
ENST00000523207.1:c.580-69663dup	ENSP00000430846.1:n.580-69663dup
NM_004770.2:c.580-69663dup	NP_004761.2:n.580-69663dup
XM_017013981.1:c.-157+2568dup	XP_016869470.1:n.-157+2568dup
XR_001745620.1:n.1141-69663dup
XR_001745621.1:n.1141-69663dup
NM_004770.3:c.580-69663dup MANE Select	NP_004761.2:n.580-69663dup