Canonical Allele Identifier: CA179627968

Gene: KCNB2

Linked Data

• dbSNP Id: rs938793303
• MyVariant Identifiers: chr8:g.73778469_73778470del (hg19) ; chr8:g.72866234_72866235del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.72866242_72866243del , CM000670.2:g.72866242_72866243del	GRCh38
NC_000008.10:g.73778477_73778478del , CM000670.1:g.73778477_73778478del	GRCh37
NC_000008.9:g.73941031_73941032del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000523207.2:c.580-69693_580-69692del MANE Select	ENSP00000430846.1:n.580-69693_580-69692del
ENST00000523207.1:c.580-69693_580-69692del	ENSP00000430846.1:n.580-69693_580-69692del
NM_004770.2:c.580-69693_580-69692del	NP_004761.2:n.580-69693_580-69692del
XM_017013981.1:c.-157+2538_-157+2539del	XP_016869470.1:n.-157+2538_-157+2539del
XR_001745620.1:n.1141-69693_1141-69692del
XR_001745621.1:n.1141-69693_1141-69692del
NM_004770.3:c.580-69693_580-69692del MANE Select	NP_004761.2:n.580-69693_580-69692del