Canonical Allele Identifier: CA7684634

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78618919T>C , CM000677.2:g.78618919T>C	GRCh38
NC_000015.9:g.78911261T>C , CM000677.1:g.78911261T>C	GRCh37
NC_000015.8:g.76698316T>C	NCBI36
NG_016143.1:g.7377A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000743.5:c.83-4A>G MANE Select	NP_000734.2:n.83-4A>G
ENST00000326828.6:c.83-4A>G MANE Select	ENSP00000315602.5:n.83-4A>G
NM_000743.4:c.83-4A>G	NP_000734.2:n.83-4A>G
NM_001166694.1:c.83-4A>G	NP_001160166.1:n.83-4A>G
NM_001166694.2:c.83-4A>G	NP_001160166.1:n.83-4A>G
NR_046313.1:n.584-4A>G
NR_046313.2:n.285-4A>G
ENST00000326828.5:c.83-4A>G	ENSP00000315602.5:n.83-4A>G
ENST00000348639.7:c.83-4A>G	ENSP00000267951.4:n.83-4A>G
ENST00000559080.1:c.-123A>G	ENSP00000453993.1:n.-123A>G
ENST00000559658.5:c.83-4A>G	ENSP00000452896.1:n.83-4A>G
ENST00000559941.1:n.526-4A>G
ENST00000561128.1:n.78-4A>G
XM_006720382.1:c.-119-4A>G	XP_006720445.1:n.-119-4A>G
XM_006720382.3:c.-119-4A>G	XP_006720445.1:n.-119-4A>G
XM_011521173.1:c.2-4A>G	XP_011519475.1:n.2-4A>G