Canonical Allele Identifier: CA1793441556

Gene: KCNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.72866378_72866379delinsCT , CM000670.2:g.72866378_72866379delinsCT	GRCh38
NC_000008.10:g.73778613_73778614delinsCT , CM000670.1:g.73778613_73778614delinsCT	GRCh37
NC_000008.9:g.73941167_73941168delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000523207.2:c.580-69557_580-69556delinsCT MANE Select	ENSP00000430846.1:n.580-69557_580-69556delinsCT
ENST00000523207.1:c.580-69557_580-69556delinsCT	ENSP00000430846.1:n.580-69557_580-69556delinsCT
NM_004770.2:c.580-69557_580-69556delinsCT	NP_004761.2:n.580-69557_580-69556delinsCT
XM_017013981.1:c.-157+2674_-157+2675delinsCT	XP_016869470.1:n.-157+2674_-157+2675delinsCT
XR_001745620.1:n.1141-69557_1141-69556delinsCT
XR_001745621.1:n.1141-69557_1141-69556delinsCT
NM_004770.3:c.580-69557_580-69556delinsCT MANE Select	NP_004761.2:n.580-69557_580-69556delinsCT