Canonical Allele Identifier: CA1793441530

Gene: KCNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.72866316_72866317delinsCT , CM000670.2:g.72866316_72866317delinsCT	GRCh38
NC_000008.10:g.73778551_73778552delinsCT , CM000670.1:g.73778551_73778552delinsCT	GRCh37
NC_000008.9:g.73941105_73941106delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000523207.2:c.580-69619_580-69618delinsCT MANE Select	ENSP00000430846.1:n.580-69619_580-69618delinsCT
ENST00000523207.1:c.580-69619_580-69618delinsCT	ENSP00000430846.1:n.580-69619_580-69618delinsCT
NM_004770.2:c.580-69619_580-69618delinsCT	NP_004761.2:n.580-69619_580-69618delinsCT
XM_017013981.1:c.-157+2612_-157+2613delinsCT	XP_016869470.1:n.-157+2612_-157+2613delinsCT
XR_001745620.1:n.1141-69619_1141-69618delinsCT
XR_001745621.1:n.1141-69619_1141-69618delinsCT
NM_004770.3:c.580-69619_580-69618delinsCT MANE Select	NP_004761.2:n.580-69619_580-69618delinsCT