Canonical Allele Identifier: CA7684648

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78620702T>C , CM000677.2:g.78620702T>C	GRCh38
NC_000015.9:g.78913044T>C , CM000677.1:g.78913044T>C	GRCh37
NC_000015.8:g.76700099T>C	NCBI36
NG_016143.1:g.5594A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000743.5:c.82+11A>G MANE Select	NP_000734.2:n.82+11A>G
ENST00000326828.6:c.82+11A>G MANE Select	ENSP00000315602.5:n.82+11A>G
NM_000743.4:c.82+11A>G	NP_000734.2:n.82+11A>G
NM_001166694.1:c.82+11A>G	NP_001160166.1:n.82+11A>G
NM_001166694.2:c.82+11A>G	NP_001160166.1:n.82+11A>G
NR_046313.1:n.583+11A>G
NR_046313.2:n.284+11A>G
ENST00000326828.5:c.82+11A>G	ENSP00000315602.5:n.82+11A>G
ENST00000348639.7:c.82+11A>G	ENSP00000267951.4:n.82+11A>G
ENST00000559658.5:c.82+11A>G	ENSP00000452896.1:n.82+11A>G
ENST00000561128.1:n.77+11A>G