Canonical Allele Identifier: CA1423682053

Gene: KCNMB3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179243013T= , CM000665.2:g.179243013T=	GRCh38
NC_000003.11:g.178960801T= , CM000665.1:g.178960801T=	GRCh37
NC_000003.10:g.180443495T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392685.7:c.719A= MANE Select	ENSP00000376451.2:p.Tyr240=
ENST00000314235.9:c.731A=	ENSP00000319370.5:p.Tyr244=
ENST00000349697.2:c.725A=	ENSP00000327866.2:p.Tyr242=
ENST00000392685.6:c.719A=	ENSP00000376451.2:p.Tyr240=
ENST00000392686.6:c.665A=	ENSP00000376452.2:p.Tyr222=
ENST00000485523.5:c.665A=	ENSP00000418536.1:p.Tyr222=
ENST00000486944.2:c.152+120A=	ENSP00000479162.1:n.152+120A=
ENST00000497599.5:c.453+1482A=	ENSP00000417091.1:n.453+1482A=
NM_001163677.1:c.453+1482A=	NP_001157149.1:n.453+1482A=
NM_014407.3:c.731A=	NP_055222.3:p.Tyr244=
NM_171828.2:c.725A=	NP_741979.1:p.Tyr242=
NM_171829.2:c.665A=	NP_741980.1:p.Tyr222=
NM_171830.1:c.719A=	NP_741981.1:p.Tyr240=
NR_028135.1:n.1607A=
NM_001163677.2:c.453+1482A=	NP_001157149.1:n.453+1482A=
NM_171828.3:c.725A=	NP_741979.1:p.Tyr242=
NM_171829.3:c.665A=	NP_741980.1:p.Tyr222=
NR_028135.2:n.1607A=
NM_171830.2:c.719A= MANE Select	NP_741981.1:p.Tyr240=