Canonical Allele Identifier: CA1423682066

Gene: KCNMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179243043G= , CM000665.2:g.179243043G=	GRCh38
NC_000003.11:g.178960831G= , CM000665.1:g.178960831G=	GRCh37
NC_000003.10:g.180443525G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392685.7:c.689C= MANE Select	ENSP00000376451.2:p.Thr230=
ENST00000314235.9:c.701C=	ENSP00000319370.5:p.Thr234=
ENST00000349697.2:c.695C=	ENSP00000327866.2:p.Thr232=
ENST00000392685.6:c.689C=	ENSP00000376451.2:p.Thr230=
ENST00000392686.6:c.635C=	ENSP00000376452.2:p.Thr212=
ENST00000485523.5:c.635C=	ENSP00000418536.1:p.Thr212=
ENST00000486944.2:c.152+90C=	ENSP00000479162.1:n.152+90C=
ENST00000497599.5:c.453+1452C=	ENSP00000417091.1:n.453+1452C=
NM_001163677.1:c.453+1452C=	NP_001157149.1:n.453+1452C=
NM_014407.3:c.701C=	NP_055222.3:p.Thr234=
NM_171828.2:c.695C=	NP_741979.1:p.Thr232=
NM_171829.2:c.635C=	NP_741980.1:p.Thr212=
NM_171830.1:c.689C=	NP_741981.1:p.Thr230=
NR_028135.1:n.1577C=
NM_001163677.2:c.453+1452C=	NP_001157149.1:n.453+1452C=
NM_171828.3:c.695C=	NP_741979.1:p.Thr232=
NM_171829.3:c.635C=	NP_741980.1:p.Thr212=
NR_028135.2:n.1577C=
NM_171830.2:c.689C= MANE Select	NP_741981.1:p.Thr230=