Canonical Allele Identifier: CA1793441477
Gene: KCNB2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.72866220A= , CM000670.2:g.72866220A= GRCh38
NC_000008.10:g.73778455A= , CM000670.1:g.73778455A= GRCh37
NC_000008.9:g.73941009A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000523207.2:c.580-69715A= MANE Select ENSP00000430846.1:n.580-69715A=
ENST00000523207.1:c.580-69715A= ENSP00000430846.1:n.580-69715A=
NM_004770.2:c.580-69715A= NP_004761.2:n.580-69715A=
XM_017013981.1:c.-157+2516A= XP_016869470.1:n.-157+2516A=
XR_001745620.1:n.1141-69715A=
XR_001745621.1:n.1141-69715A=
NM_004770.3:c.580-69715A= MANE Select NP_004761.2:n.580-69715A=
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