Canonical Allele Identifier: CA2502409668

Gene: KCNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.72866332_72866333insTAC , CM000670.2:g.72866332_72866333insTAC	GRCh38
NC_000008.10:g.73778567_73778568insTAC , CM000670.1:g.73778567_73778568insTAC	GRCh37
NC_000008.9:g.73941121_73941122insTAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000523207.2:c.580-69603_580-69602insTAC MANE Select	ENSP00000430846.1:n.580-69603_580-69602insTAC
ENST00000523207.1:c.580-69603_580-69602insTAC	ENSP00000430846.1:n.580-69603_580-69602insTAC
NM_004770.2:c.580-69603_580-69602insTAC	NP_004761.2:n.580-69603_580-69602insTAC
XM_017013981.1:c.-157+2628_-157+2629insTAC	XP_016869470.1:n.-157+2628_-157+2629insTAC
XR_001745620.1:n.1141-69603_1141-69602insTAC
XR_001745621.1:n.1141-69603_1141-69602insTAC
NM_004770.3:c.580-69603_580-69602insTAC MANE Select	NP_004761.2:n.580-69603_580-69602insTAC