Canonical Allele Identifier: CA1793441565

Gene: KCNB2

Linked Data

• dbSNP Id: rs1805519394

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.72866398_72866401del , CM000670.2:g.72866398_72866401del	GRCh38
NC_000008.10:g.73778633_73778636del , CM000670.1:g.73778633_73778636del	GRCh37
NC_000008.9:g.73941187_73941190del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000523207.2:c.580-69537_580-69534del MANE Select	ENSP00000430846.1:n.580-69537_580-69534del
ENST00000523207.1:c.580-69537_580-69534del	ENSP00000430846.1:n.580-69537_580-69534del
NM_004770.2:c.580-69537_580-69534del	NP_004761.2:n.580-69537_580-69534del
XM_017013981.1:c.-157+2694_-157+2697del	XP_016869470.1:n.-157+2694_-157+2697del
XR_001745620.1:n.1141-69537_1141-69534del
XR_001745621.1:n.1141-69537_1141-69534del
NM_004770.3:c.580-69537_580-69534del MANE Select	NP_004761.2:n.580-69537_580-69534del