Canonical Allele Identifier: CA1793441538
Gene: KCNB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.72866343A= , CM000670.2:g.72866343A= GRCh38
NC_000008.10:g.73778578A= , CM000670.1:g.73778578A= GRCh37
NC_000008.9:g.73941132A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000523207.2:c.580-69592A= MANE Select ENSP00000430846.1:n.580-69592A=
ENST00000523207.1:c.580-69592A= ENSP00000430846.1:n.580-69592A=
NM_004770.2:c.580-69592A= NP_004761.2:n.580-69592A=
XM_017013981.1:c.-157+2639A= XP_016869470.1:n.-157+2639A=
XR_001745620.1:n.1141-69592A=
XR_001745621.1:n.1141-69592A=
NM_004770.3:c.580-69592A= MANE Select NP_004761.2:n.580-69592A=