Canonical Allele Identifier: CA1793441516
Gene: KCNB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.72866307_72866310delinsCATT , CM000670.2:g.72866307_72866310delinsCATT GRCh38
NC_000008.10:g.73778542_73778545delinsCATT , CM000670.1:g.73778542_73778545delinsCATT GRCh37
NC_000008.9:g.73941096_73941099delinsCATT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000523207.2:c.580-69628_580-69625delinsCATT MANE Select ENSP00000430846.1:n.580-69628_580-69625de...
ENST00000523207.1:c.580-69628_580-69625delinsCATT ENSP00000430846.1:n.580-69628_580-69625de...
NM_004770.2:c.580-69628_580-69625delinsCATT NP_004761.2:n.580-69628_580-69625delinsCA...
XM_017013981.1:c.-157+2603_-157+2606delinsCATT XP_016869470.1:n.-157+2603_-157+2606delin...
XR_001745620.1:n.1141-69628_1141-69625delinsCATT
XR_001745621.1:n.1141-69628_1141-69625delinsCATT
NM_004770.3:c.580-69628_580-69625delinsCATT MANE Select NP_004761.2:n.580-69628_580-69625delinsCA...