Canonical Allele Identifier: CA355288411
Gene: KCNMB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179243018T>G , CM000665.2:g.179243018T>G GRCh38
NC_000003.11:g.178960806T>G , CM000665.1:g.178960806T>G GRCh37
NC_000003.10:g.180443500T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000392685.7:c.714A>C MANE Select ENSP00000376451.2:p.Glu238Asp
ENST00000314235.9:c.726A>C ENSP00000319370.5:p.Glu242Asp
ENST00000349697.2:c.720A>C ENSP00000327866.2:p.Glu240Asp
ENST00000392685.6:c.714A>C ENSP00000376451.2:p.Glu238Asp
ENST00000392686.6:c.660A>C ENSP00000376452.2:p.Glu220Asp
ENST00000485523.5:c.660A>C ENSP00000418536.1:p.Glu220Asp
ENST00000486944.2:c.152+115A>C ENSP00000479162.1:n.152+115A>C
ENST00000497599.5:c.453+1477A>C ENSP00000417091.1:n.453+1477A>C
NM_001163677.1:c.453+1477A>C NP_001157149.1:n.453+1477A>C
NM_014407.3:c.726A>C NP_055222.3:p.Glu242Asp
NM_171828.2:c.720A>C NP_741979.1:p.Glu240Asp
NM_171829.2:c.660A>C NP_741980.1:p.Glu220Asp
NM_171830.1:c.714A>C NP_741981.1:p.Glu238Asp
NR_028135.1:n.1602A>C
NM_001163677.2:c.453+1477A>C NP_001157149.1:n.453+1477A>C
NM_171828.3:c.720A>C NP_741979.1:p.Glu240Asp
NM_171829.3:c.660A>C NP_741980.1:p.Glu220Asp
NR_028135.2:n.1602A>C
NM_171830.2:c.714A>C MANE Select NP_741981.1:p.Glu238Asp