Canonical Allele Identifier: CA355288419
Gene: KCNMB3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.179243021A>T , CM000665.2:g.179243021A>T GRCh38
NC_000003.11:g.178960809A>T , CM000665.1:g.178960809A>T GRCh37
NC_000003.10:g.180443503A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000392685.7:c.711T>A MANE Select ENSP00000376451.2:p.Cys237Ter
ENST00000314235.9:c.723T>A ENSP00000319370.5:p.Cys241Ter
ENST00000349697.2:c.717T>A ENSP00000327866.2:p.Cys239Ter
ENST00000392685.6:c.711T>A ENSP00000376451.2:p.Cys237Ter
ENST00000392686.6:c.657T>A ENSP00000376452.2:p.Cys219Ter
ENST00000485523.5:c.657T>A ENSP00000418536.1:p.Cys219Ter
ENST00000486944.2:c.152+112T>A ENSP00000479162.1:n.152+112T>A
ENST00000497599.5:c.453+1474T>A ENSP00000417091.1:n.453+1474T>A
NM_001163677.1:c.453+1474T>A NP_001157149.1:n.453+1474T>A
NM_014407.3:c.723T>A NP_055222.3:p.Cys241Ter
NM_171828.2:c.717T>A NP_741979.1:p.Cys239Ter
NM_171829.2:c.657T>A NP_741980.1:p.Cys219Ter
NM_171830.1:c.711T>A NP_741981.1:p.Cys237Ter
NR_028135.1:n.1599T>A
NM_001163677.2:c.453+1474T>A NP_001157149.1:n.453+1474T>A
NM_171828.3:c.717T>A NP_741979.1:p.Cys239Ter
NM_171829.3:c.657T>A NP_741980.1:p.Cys219Ter
NR_028135.2:n.1599T>A
NM_171830.2:c.711T>A MANE Select NP_741981.1:p.Cys237Ter