Canonical Allele Identifier: CA1793441582
Gene: KCNB2 HGNC NCBI

Linked Data

dbSNP Id: rs1805520199
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.72866429dup , CM000670.2:g.72866429dup GRCh38
NC_000008.10:g.73778664dup , CM000670.1:g.73778664dup GRCh37
NC_000008.9:g.73941218dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000523207.2:c.580-69506dup MANE Select ENSP00000430846.1:n.580-69506dup
ENST00000523207.1:c.580-69506dup ENSP00000430846.1:n.580-69506dup
NM_004770.2:c.580-69506dup NP_004761.2:n.580-69506dup
XM_017013981.1:c.-157+2725dup XP_016869470.1:n.-157+2725dup
XR_001745620.1:n.1141-69506dup
XR_001745621.1:n.1141-69506dup
NM_004770.3:c.580-69506dup MANE Select NP_004761.2:n.580-69506dup
Search 100 bp 5'
Search 100 bp 3'