Canonical Allele Identifier: CA1793441548
Gene: KCNB2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.72866366C= , CM000670.2:g.72866366C= GRCh38
NC_000008.10:g.73778601C= , CM000670.1:g.73778601C= GRCh37
NC_000008.9:g.73941155C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000523207.2:c.580-69569C= MANE Select ENSP00000430846.1:n.580-69569C=
ENST00000523207.1:c.580-69569C= ENSP00000430846.1:n.580-69569C=
NM_004770.2:c.580-69569C= NP_004761.2:n.580-69569C=
XM_017013981.1:c.-157+2662C= XP_016869470.1:n.-157+2662C=
XR_001745620.1:n.1141-69569C=
XR_001745621.1:n.1141-69569C=
NM_004770.3:c.580-69569C= MANE Select NP_004761.2:n.580-69569C=
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