Canonical Allele Identifier: CA1793441489
Gene: KCNB2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.72866237G= , CM000670.2:g.72866237G= GRCh38
NC_000008.10:g.73778472G= , CM000670.1:g.73778472G= GRCh37
NC_000008.9:g.73941026G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000523207.2:c.580-69698G= MANE Select ENSP00000430846.1:n.580-69698G=
ENST00000523207.1:c.580-69698G= ENSP00000430846.1:n.580-69698G=
NM_004770.2:c.580-69698G= NP_004761.2:n.580-69698G=
XM_017013981.1:c.-157+2533G= XP_016869470.1:n.-157+2533G=
XR_001745620.1:n.1141-69698G=
XR_001745621.1:n.1141-69698G=
NM_004770.3:c.580-69698G= MANE Select NP_004761.2:n.580-69698G=
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