Canonical Allele Identifier: CA1793441398

Gene: KCNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.72866042_72866043delinsAT , CM000670.2:g.72866042_72866043delinsAT	GRCh38
NC_000008.10:g.73778277_73778278delinsAT , CM000670.1:g.73778277_73778278delinsAT	GRCh37
NC_000008.9:g.73940831_73940832delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000523207.2:c.580-69893_580-69892delinsAT MANE Select	ENSP00000430846.1:n.580-69893_580-69892delinsAT
ENST00000523207.1:c.580-69893_580-69892delinsAT	ENSP00000430846.1:n.580-69893_580-69892delinsAT
NM_004770.2:c.580-69893_580-69892delinsAT	NP_004761.2:n.580-69893_580-69892delinsAT
XM_017013981.1:c.-157+2338_-157+2339delinsAT	XP_016869470.1:n.-157+2338_-157+2339delinsAT
XR_001745620.1:n.1141-69893_1141-69892delinsAT
XR_001745621.1:n.1141-69893_1141-69892delinsAT
NM_004770.3:c.580-69893_580-69892delinsAT MANE Select	NP_004761.2:n.580-69893_580-69892delinsAT