Canonical Allele Identifier: CA855041786
Gene: KCNB2 HGNC NCBI

Linked Data

dbSNP Id: rs1277620881

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.72866461A>G , CM000670.2:g.72866461A>G GRCh38
NC_000008.10:g.73778696A>G , CM000670.1:g.73778696A>G GRCh37
NC_000008.9:g.73941250A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000523207.2:c.580-69474A>G MANE Select ENSP00000430846.1:n.580-69474A>G
ENST00000523207.1:c.580-69474A>G ENSP00000430846.1:n.580-69474A>G
NM_004770.2:c.580-69474A>G NP_004761.2:n.580-69474A>G
XM_017013981.1:c.-157+2757A>G XP_016869470.1:n.-157+2757A>G
XR_001745620.1:n.1141-69474A>G
XR_001745621.1:n.1141-69474A>G
NM_004770.3:c.580-69474A>G MANE Select NP_004761.2:n.580-69474A>G