Canonical Allele Identifier: CA2189575305

Gene: CHRNB4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78629887T= , CM000677.2:g.78629887T=	GRCh38
NC_000015.9:g.78922229T= , CM000677.1:g.78922229T=	GRCh37
NC_000015.8:g.76709284T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_000750.5:c.418A= MANE Select	NP_000741.1:p.Ser140=
ENST00000261751.8:c.418A= MANE Select	ENSP00000261751.3:p.Ser140=
NM_000750.3:c.418A=	NP_000741.1:p.Ser140=
NM_000750.4:c.418A=	NP_000741.1:p.Ser140=
NM_001256567.1:c.359+1189A=	NP_001243496.1:n.359+1189A=
NM_001256567.2:c.359+1189A=	NP_001243496.1:n.359+1189A=
NM_001256567.3:c.359+1189A=	NP_001243496.1:n.359+1189A=
ENST00000261751.7:c.418A=	ENSP00000261751.3:p.Ser140=
ENST00000412074.6:c.359+1189A=	ENSP00000416386.2:n.359+1189A=
ENST00000559849.5:c.*474A=	ENSP00000457404.1:n.*474A=
XM_011521181.1:c.601A=	XP_011519483.1:p.Ser201=
XM_011521182.1:c.601A=	XP_011519484.1:p.Ser201=
XM_011521183.1:c.601A=	XP_011519485.1:p.Ser201=
XM_011521184.1:c.601A=	XP_011519486.1:p.Ser201=
XM_011521185.1:c.601A=	XP_011519487.1:p.Ser201=
XM_011521186.1:c.409A=	XP_011519488.1:p.Ser137=
XM_011521186.2:c.409A=	XP_011519488.1:p.Ser137=
XM_011521187.1:c.409A=	XP_011519489.1:p.Ser137=
XM_011521187.2:c.409A=	XP_011519489.1:p.Ser137=
XM_011521188.1:c.328A=	XP_011519490.1:p.Ser110=
XM_011521189.1:c.253A=	XP_011519491.1:p.Ser85=
XM_011521190.1:c.196A=	XP_011519492.1:p.Ser66=
XM_011521190.2:c.196A=	XP_011519492.1:p.Ser66=
XM_011521191.1:c.196A=	XP_011519493.1:p.Ser66=
XM_011521191.2:c.196A=	XP_011519493.1:p.Ser66=
XM_011521192.1:c.-129A=	XP_011519494.1:n.-129A=
XM_011521192.2:c.-129A=	XP_011519494.1:n.-129A=
XM_011521193.1:c.542+1189A=	XP_011519495.1:n.542+1189A=
XM_017021885.1:c.328A=	XP_016877374.1:p.Ser110=
XM_017021886.1:c.328A=	XP_016877375.1:p.Ser110=
XM_017021887.1:c.418A=	XP_016877376.1:p.Ser140=
XM_017021888.1:c.418A=	XP_016877377.1:p.Ser140=
XM_017021889.2:c.418A=	XP_016877378.1:p.Ser140=