Canonical Allele Identifier: CA2629793467

Gene: CHRNA3

Linked Data

• gnomAD v4: 15-78595972-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78595972G>C , CM000677.2:g.78595972G>C	GRCh38
NC_000015.9:g.78888314G>C , CM000677.1:g.78888314G>C	GRCh37
NC_000015.8:g.76675369G>C	NCBI36
NG_016143.1:g.30324C>G
NG_023328.1:g.35453G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.*632C>G MANE Select	ENSP00000315602.5:n.*632C>G
ENST00000326828.5:c.*632C>G	ENSP00000315602.5:n.*632C>G
ENST00000348639.7:c.1390-2781C>G	ENSP00000267951.4:n.1390-2781C>G
ENST00000559002.5:n.193+568C>G
ENST00000559658.5:c.*64+568C>G	ENSP00000452896.1:n.*64+568C>G
NM_000743.4:c.*632C>G	NP_000734.2:n.*632C>G
NM_001166694.1:c.1390-2781C>G	NP_001160166.1:n.1390-2781C>G
NR_046313.1:n.2083+568C>G
XM_006720382.1:c.*632C>G	XP_006720445.1:n.*632C>G
XM_011521173.1:c.*632C>G	XP_011519475.1:n.*632C>G
XM_006720382.3:c.*632C>G	XP_006720445.1:n.*632C>G
NM_000743.5:c.*632C>G MANE Select	NP_000734.2:n.*632C>G
NM_001166694.2:c.1390-2781C>G	NP_001160166.1:n.1390-2781C>G
NR_046313.2:n.1784+568C>G