Canonical Allele Identifier: CA16608469
Gene: KCNB1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.49374622T>C , CM000682.2:g.49374622T>C GRCh38
NC_000020.10:g.47991159T>C , CM000682.1:g.47991159T>C GRCh37
NC_000020.9:g.47424566T>C NCBI36
NG_041781.1:g.113023A>G
NG_041781.2:g.113023A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371741.6:c.938A>G MANE Select ENSP00000360806.3:p.His313Arg
ENST00000635878.1:c.97-75239A>G ENSP00000489908.1:n.97-75239A>G
ENST00000637341.1:n.206+42598T>C
ENST00000371741.5:c.938A>G ENSP00000360806.3:p.His313Arg
ENST00000635465.1:c.938A>G ENSP00000489193.1:p.His313Arg
NM_004975.2:c.938A>G NP_004966.1:p.His313Arg
XM_006723784.2:c.938A>G XP_006723847.1:p.His313Arg
XM_011528799.1:c.938A>G XP_011527101.1:p.His313Arg
NM_004975.3:c.938A>G NP_004966.1:p.His313Arg
XM_006723784.3:c.938A>G XP_006723847.1:p.His313Arg
XM_011528799.2:c.938A>G XP_011527101.1:p.His313Arg
XR_001754659.1:n.156+42598T>C
NM_004975.4:c.938A>G MANE Select NP_004966.1:p.His313Arg
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