Canonical Allele Identifier: CA2555174805

Gene: KCNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.72866179A>T , CM000670.2:g.72866179A>T	GRCh38
NC_000008.10:g.73778414A>T , CM000670.1:g.73778414A>T	GRCh37
NC_000008.9:g.73940968A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000523207.2:c.580-69756A>T MANE Select	ENSP00000430846.1:n.580-69756A>T
ENST00000523207.1:c.580-69756A>T	ENSP00000430846.1:n.580-69756A>T
NM_004770.2:c.580-69756A>T	NP_004761.2:n.580-69756A>T
XM_017013981.1:c.-157+2475A>T	XP_016869470.1:n.-157+2475A>T
XR_001745620.1:n.1141-69756A>T
XR_001745621.1:n.1141-69756A>T
NM_004770.3:c.580-69756A>T MANE Select	NP_004761.2:n.580-69756A>T