Canonical Allele Identifier: CA1793441550
Gene: KCNB2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.72866368A= , CM000670.2:g.72866368A= GRCh38
NC_000008.10:g.73778603A= , CM000670.1:g.73778603A= GRCh37
NC_000008.9:g.73941157A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000523207.2:c.580-69567A= MANE Select ENSP00000430846.1:n.580-69567A=
ENST00000523207.1:c.580-69567A= ENSP00000430846.1:n.580-69567A=
NM_004770.2:c.580-69567A= NP_004761.2:n.580-69567A=
XM_017013981.1:c.-157+2664A= XP_016869470.1:n.-157+2664A=
XR_001745620.1:n.1141-69567A=
XR_001745621.1:n.1141-69567A=
NM_004770.3:c.580-69567A= MANE Select NP_004761.2:n.580-69567A=
Search 100 bp 5'
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