Canonical Allele Identifier: CA355288471
Gene: KCNMB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179243048T>A , CM000665.2:g.179243048T>A GRCh38
NC_000003.11:g.178960836T>A , CM000665.1:g.178960836T>A GRCh37
NC_000003.10:g.180443530T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000392685.7:c.684A>T MANE Select ENSP00000376451.2:p.Arg228Ser
ENST00000314235.9:c.696A>T ENSP00000319370.5:p.Arg232Ser
ENST00000349697.2:c.690A>T ENSP00000327866.2:p.Arg230Ser
ENST00000392685.6:c.684A>T ENSP00000376451.2:p.Arg228Ser
ENST00000392686.6:c.630A>T ENSP00000376452.2:p.Arg210Ser
ENST00000485523.5:c.630A>T ENSP00000418536.1:p.Arg210Ser
ENST00000486944.2:c.152+85A>T ENSP00000479162.1:n.152+85A>T
ENST00000497599.5:c.453+1447A>T ENSP00000417091.1:n.453+1447A>T
NM_001163677.1:c.453+1447A>T NP_001157149.1:n.453+1447A>T
NM_014407.3:c.696A>T NP_055222.3:p.Arg232Ser
NM_171828.2:c.690A>T NP_741979.1:p.Arg230Ser
NM_171829.2:c.630A>T NP_741980.1:p.Arg210Ser
NM_171830.1:c.684A>T NP_741981.1:p.Arg228Ser
NR_028135.1:n.1572A>T
NM_001163677.2:c.453+1447A>T NP_001157149.1:n.453+1447A>T
NM_171828.3:c.690A>T NP_741979.1:p.Arg230Ser
NM_171829.3:c.630A>T NP_741980.1:p.Arg210Ser
NR_028135.2:n.1572A>T
NM_171830.2:c.684A>T MANE Select NP_741981.1:p.Arg228Ser