Canonical Allele Identifier: CA1793441498

Gene: KCNB2

Linked Data

• dbSNP Id: rs1805516293

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.72866261T>G , CM000670.2:g.72866261T>G	GRCh38
NC_000008.10:g.73778496T>G , CM000670.1:g.73778496T>G	GRCh37
NC_000008.9:g.73941050T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000523207.2:c.580-69674T>G MANE Select	ENSP00000430846.1:n.580-69674T>G
ENST00000523207.1:c.580-69674T>G	ENSP00000430846.1:n.580-69674T>G
NM_004770.2:c.580-69674T>G	NP_004761.2:n.580-69674T>G
XM_017013981.1:c.-157+2557T>G	XP_016869470.1:n.-157+2557T>G
XR_001745620.1:n.1141-69674T>G
XR_001745621.1:n.1141-69674T>G
NM_004770.3:c.580-69674T>G MANE Select	NP_004761.2:n.580-69674T>G