Canonical Allele Identifier: CA14086647

Gene: CHRNB4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78633676T>C , CM000677.2:g.78633676T>C	GRCh38
NC_000015.9:g.78926018T>C , CM000677.1:g.78926018T>C	GRCh37
NC_000015.8:g.76713073T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261751.8:c.204+1763A>G MANE Select	ENSP00000261751.3:n.204+1763A>G
ENST00000261751.7:c.204+1763A>G	ENSP00000261751.3:n.204+1763A>G
ENST00000412074.6:c.204+1763A>G	ENSP00000416386.2:n.204+1763A>G
ENST00000559849.5:c.*112+946A>G	ENSP00000457404.1:n.*112+946A>G
ENST00000560511.5:n.558+1763A>G
NM_000750.3:c.204+1763A>G	NP_000741.1:n.204+1763A>G
NM_001256567.1:c.204+1763A>G	NP_001243496.1:n.204+1763A>G
XM_011521181.1:c.387+1763A>G	XP_011519483.1:n.387+1763A>G
XM_011521182.1:c.387+1763A>G	XP_011519484.1:n.387+1763A>G
XM_011521183.1:c.387+1763A>G	XP_011519485.1:n.387+1763A>G
XM_011521184.1:c.387+1763A>G	XP_011519486.1:n.387+1763A>G
XM_011521185.1:c.387+1763A>G	XP_011519487.1:n.387+1763A>G
XM_011521186.1:c.195+1763A>G	XP_011519488.1:n.195+1763A>G
XM_011521187.1:c.195+1763A>G	XP_011519489.1:n.195+1763A>G
XM_011521188.1:c.114+1763A>G	XP_011519490.1:n.114+1763A>G
XM_011521189.1:c.-34A>G	XP_011519491.1:n.-34A>G
XM_011521190.1:c.-19+946A>G	XP_011519492.1:n.-19+946A>G
XM_011521191.1:c.-18-2344A>G	XP_011519493.1:n.-18-2344A>G
XM_011521192.1:c.-491+1763A>G	XP_011519494.1:n.-491+1763A>G
XM_011521193.1:c.387+1763A>G	XP_011519495.1:n.387+1763A>G
NM_000750.4:c.204+1763A>G	NP_000741.1:n.204+1763A>G
NM_001256567.2:c.204+1763A>G	NP_001243496.1:n.204+1763A>G
XM_011521186.2:c.195+1763A>G	XP_011519488.1:n.195+1763A>G
XM_011521187.2:c.195+1763A>G	XP_011519489.1:n.195+1763A>G
XM_011521190.2:c.-19+946A>G	XP_011519492.1:n.-19+946A>G
XM_011521191.2:c.-18-2344A>G	XP_011519493.1:n.-18-2344A>G
XM_011521192.2:c.-491+1763A>G	XP_011519494.1:n.-491+1763A>G
XM_017021885.1:c.114+1763A>G	XP_016877374.1:n.114+1763A>G
XM_017021886.1:c.114+1763A>G	XP_016877375.1:n.114+1763A>G
XM_017021887.1:c.204+1763A>G	XP_016877376.1:n.204+1763A>G
XM_017021888.1:c.204+1763A>G	XP_016877377.1:n.204+1763A>G
XM_017021889.2:c.204+1763A>G	XP_016877378.1:n.204+1763A>G
NM_000750.5:c.204+1763A>G MANE Select	NP_000741.1:n.204+1763A>G
NM_001256567.3:c.204+1763A>G	NP_001243496.1:n.204+1763A>G