Canonical Allele Identifier: CA1423682073

Gene: KCNMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179243063A= , CM000665.2:g.179243063A=	GRCh38
NC_000003.11:g.178960851A= , CM000665.1:g.178960851A=	GRCh37
NC_000003.10:g.180443545A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392685.7:c.669T= MANE Select	ENSP00000376451.2:p.Ile223=
ENST00000314235.9:c.681T=	ENSP00000319370.5:p.Ile227=
ENST00000349697.2:c.675T=	ENSP00000327866.2:p.Ile225=
ENST00000392685.6:c.669T=	ENSP00000376451.2:p.Ile223=
ENST00000392686.6:c.615T=	ENSP00000376452.2:p.Ile205=
ENST00000485523.5:c.615T=	ENSP00000418536.1:p.Ile205=
ENST00000486944.2:c.152+70T=	ENSP00000479162.1:n.152+70T=
ENST00000497599.5:c.453+1432T=	ENSP00000417091.1:n.453+1432T=
NM_001163677.1:c.453+1432T=	NP_001157149.1:n.453+1432T=
NM_014407.3:c.681T=	NP_055222.3:p.Ile227=
NM_171828.2:c.675T=	NP_741979.1:p.Ile225=
NM_171829.2:c.615T=	NP_741980.1:p.Ile205=
NM_171830.1:c.669T=	NP_741981.1:p.Ile223=
NR_028135.1:n.1557T=
NM_001163677.2:c.453+1432T=	NP_001157149.1:n.453+1432T=
NM_171828.3:c.675T=	NP_741979.1:p.Ile225=
NM_171829.3:c.615T=	NP_741980.1:p.Ile205=
NR_028135.2:n.1557T=
NM_171830.2:c.669T= MANE Select	NP_741981.1:p.Ile223=