Canonical Allele Identifier: CA16043105
Gene: KCNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 373805
ClinVar RCV Id: RCV000413312 RCV000699040
dbSNP Id: rs1057518621
COSMIC: COSM1027866
MyVariant Identifiers: chr20:g.47991189C>T (hg19) chr20:g.49374652C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.49374652C>T , CM000682.2:g.49374652C>T GRCh38
NC_000020.10:g.47991189C>T , CM000682.1:g.47991189C>T GRCh37
NC_000020.9:g.47424596C>T NCBI36
NG_041781.1:g.112993G>A
NG_041781.2:g.112993G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371741.6:c.908G>A MANE Select ENSP00000360806.3:p.Arg303Gln
ENST00000635878.1:c.97-75269G>A ENSP00000489908.1:n.97-75269G>A
ENST00000637341.1:n.206+42628C>T
ENST00000371741.5:c.908G>A ENSP00000360806.3:p.Arg303Gln
ENST00000635465.1:c.908G>A ENSP00000489193.1:p.Arg303Gln
NM_004975.2:c.908G>A NP_004966.1:p.Arg303Gln
XM_006723784.2:c.908G>A XP_006723847.1:p.Arg303Gln
XM_011528799.1:c.908G>A XP_011527101.1:p.Arg303Gln
NM_004975.3:c.908G>A NP_004966.1:p.Arg303Gln
XM_006723784.3:c.908G>A XP_006723847.1:p.Arg303Gln
XM_011528799.2:c.908G>A XP_011527101.1:p.Arg303Gln
XR_001754659.1:n.156+42628C>T
NM_004975.4:c.908G>A MANE Select NP_004966.1:p.Arg303Gln
Search 100 bp 5'
Search 100 bp 3'