Canonical Allele Identifier: CA1793441557

Gene: KCNB2

Linked Data

• dbSNP Id: rs1805518882

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.72866379del , CM000670.2:g.72866379del	GRCh38
NC_000008.10:g.73778614del , CM000670.1:g.73778614del	GRCh37
NC_000008.9:g.73941168del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000523207.2:c.580-69556del MANE Select	ENSP00000430846.1:n.580-69556del
ENST00000523207.1:c.580-69556del	ENSP00000430846.1:n.580-69556del
NM_004770.2:c.580-69556del	NP_004761.2:n.580-69556del
XM_017013981.1:c.-157+2675del	XP_016869470.1:n.-157+2675del
XR_001745620.1:n.1141-69556del
XR_001745621.1:n.1141-69556del
NM_004770.3:c.580-69556del MANE Select	NP_004761.2:n.580-69556del