Canonical Allele Identifier: CA1793441657

Gene: KCNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.72866591_72866592delinsTG , CM000670.2:g.72866591_72866592delinsTG	GRCh38
NC_000008.10:g.73778826_73778827delinsTG , CM000670.1:g.73778826_73778827delinsTG	GRCh37
NC_000008.9:g.73941380_73941381delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000523207.2:c.580-69344_580-69343delinsTG MANE Select	ENSP00000430846.1:n.580-69344_580-69343delinsTG
ENST00000523207.1:c.580-69344_580-69343delinsTG	ENSP00000430846.1:n.580-69344_580-69343delinsTG
NM_004770.2:c.580-69344_580-69343delinsTG	NP_004761.2:n.580-69344_580-69343delinsTG
XM_017013981.1:c.-157+2887_-157+2888delinsTG	XP_016869470.1:n.-157+2887_-157+2888delinsTG
XR_001745620.1:n.1141-69344_1141-69343delinsTG
XR_001745621.1:n.1141-69344_1141-69343delinsTG
NM_004770.3:c.580-69344_580-69343delinsTG MANE Select	NP_004761.2:n.580-69344_580-69343delinsTG