Canonical Allele Identifier: CA855041655
Gene: KCNB2 HGNC NCBI

Linked Data

dbSNP Id: rs1380446004
MyVariant Identifiers: chr8:g.73778278del (hg19) chr8:g.72866043del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.72866043del , CM000670.2:g.72866043del GRCh38
NC_000008.10:g.73778278del , CM000670.1:g.73778278del GRCh37
NC_000008.9:g.73940832del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000523207.2:c.580-69892del MANE Select ENSP00000430846.1:n.580-69892del
ENST00000523207.1:c.580-69892del ENSP00000430846.1:n.580-69892del
NM_004770.2:c.580-69892del NP_004761.2:n.580-69892del
XM_017013981.1:c.-157+2339del XP_016869470.1:n.-157+2339del
XR_001745620.1:n.1141-69892del
XR_001745621.1:n.1141-69892del
NM_004770.3:c.580-69892del MANE Select NP_004761.2:n.580-69892del
Search 100 bp 5'
Search 100 bp 3'