Canonical Allele Identifier: CA179628001
Gene: KCNB2 HGNC NCBI

Linked Data

dbSNP Id: rs965668095
MyVariant Identifiers: chr8:g.73778734C>A (hg19) chr8:g.72866499C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.72866499C>A , CM000670.2:g.72866499C>A GRCh38
NC_000008.10:g.73778734C>A , CM000670.1:g.73778734C>A GRCh37
NC_000008.9:g.73941288C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000523207.2:c.580-69436C>A MANE Select ENSP00000430846.1:n.580-69436C>A
ENST00000523207.1:c.580-69436C>A ENSP00000430846.1:n.580-69436C>A
NM_004770.2:c.580-69436C>A NP_004761.2:n.580-69436C>A
XM_017013981.1:c.-157+2795C>A XP_016869470.1:n.-157+2795C>A
XR_001745620.1:n.1141-69436C>A
XR_001745621.1:n.1141-69436C>A
NM_004770.3:c.580-69436C>A MANE Select NP_004761.2:n.580-69436C>A
Search 100 bp 5'
Search 100 bp 3'