Canonical Allele Identifier: CA179627986
Gene: KCNB2 HGNC NCBI

Linked Data

dbSNP Id: rs998895079
MyVariant Identifiers: chr8:g.73778601C>G (hg19) chr8:g.72866366C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.72866366C>G , CM000670.2:g.72866366C>G GRCh38
NC_000008.10:g.73778601C>G , CM000670.1:g.73778601C>G GRCh37
NC_000008.9:g.73941155C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000523207.2:c.580-69569C>G MANE Select ENSP00000430846.1:n.580-69569C>G
ENST00000523207.1:c.580-69569C>G ENSP00000430846.1:n.580-69569C>G
NM_004770.2:c.580-69569C>G NP_004761.2:n.580-69569C>G
XM_017013981.1:c.-157+2662C>G XP_016869470.1:n.-157+2662C>G
XR_001745620.1:n.1141-69569C>G
XR_001745621.1:n.1141-69569C>G
NM_004770.3:c.580-69569C>G MANE Select NP_004761.2:n.580-69569C>G
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