Canonical Allele Identifier: CA1793441526
Gene: KCNB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.72866313_72866315delinsCTG , CM000670.2:g.72866313_72866315delinsCTG GRCh38
NC_000008.10:g.73778548_73778550delinsCTG , CM000670.1:g.73778548_73778550delinsCTG GRCh37
NC_000008.9:g.73941102_73941104delinsCTG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000523207.2:c.580-69622_580-69620delinsCTG MANE Select ENSP00000430846.1:n.580-69622_580-69620de...
ENST00000523207.1:c.580-69622_580-69620delinsCTG ENSP00000430846.1:n.580-69622_580-69620de...
NM_004770.2:c.580-69622_580-69620delinsCTG NP_004761.2:n.580-69622_580-69620delinsCT...
XM_017013981.1:c.-157+2609_-157+2611delinsCTG XP_016869470.1:n.-157+2609_-157+2611delin...
XR_001745620.1:n.1141-69622_1141-69620delinsCTG
XR_001745621.1:n.1141-69622_1141-69620delinsCTG
NM_004770.3:c.580-69622_580-69620delinsCTG MANE Select NP_004761.2:n.580-69622_580-69620delinsCT...