Canonical Allele Identifier: CA12881142
Gene: KCNB2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10504543

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.72866407G>A , CM000670.2:g.72866407G>A GRCh38
NC_000008.10:g.73778642G>A , CM000670.1:g.73778642G>A GRCh37
NC_000008.9:g.73941196G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_004770.2:c.580-69528G>A VV NP_004761.2:p.=
XM_017013981.1:c.-157+2703G>A XP_016869470.1:p.=
XR_001745620.1:n.1141-69528G>A
XR_001745621.1:n.1141-69528G>A
NM_004770.3:c.580-69528G>A VV MANE Preferred
ENST00000523207.1:c.580-69528G>A ENSP00000430846.1:p.=