Canonical Allele Identifier: CA2553359821
Gene: KCNB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.72866428_72866430del , CM000670.2:g.72866428_72866430del GRCh38
NC_000008.10:g.73778663_73778665del , CM000670.1:g.73778663_73778665del GRCh37
NC_000008.9:g.73941217_73941219del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000523207.2:c.580-69507_580-69505del MANE Select ENSP00000430846.1:n.580-69507_580-69505de...
ENST00000523207.1:c.580-69507_580-69505del ENSP00000430846.1:n.580-69507_580-69505de...
NM_004770.2:c.580-69507_580-69505del NP_004761.2:n.580-69507_580-69505del
XM_017013981.1:c.-157+2724_-157+2726del XP_016869470.1:n.-157+2724_-157+2726del
XR_001745620.1:n.1141-69507_1141-69505del
XR_001745621.1:n.1141-69507_1141-69505del
NM_004770.3:c.580-69507_580-69505del MANE Select NP_004761.2:n.580-69507_580-69505del