Canonical Allele Identifier: CA2629793443

Gene: CHRNA3

Linked Data

• gnomAD v4: 15-78595959-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78595959C>G , CM000677.2:g.78595959C>G	GRCh38
NC_000015.9:g.78888301C>G , CM000677.1:g.78888301C>G	GRCh37
NC_000015.8:g.76675356C>G	NCBI36
NG_016143.1:g.30337G>C
NG_023328.1:g.35440C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.*645G>C MANE Select	ENSP00000315602.5:n.*645G>C
ENST00000326828.5:c.*645G>C	ENSP00000315602.5:n.*645G>C
ENST00000348639.7:c.1390-2768G>C	ENSP00000267951.4:n.1390-2768G>C
ENST00000559002.5:n.193+581G>C
ENST00000559658.5:c.*64+581G>C	ENSP00000452896.1:n.*64+581G>C
NM_000743.4:c.*645G>C	NP_000734.2:n.*645G>C
NM_001166694.1:c.1390-2768G>C	NP_001160166.1:n.1390-2768G>C
NR_046313.1:n.2083+581G>C
XM_006720382.1:c.*645G>C	XP_006720445.1:n.*645G>C
XM_011521173.1:c.*645G>C	XP_011519475.1:n.*645G>C
XM_006720382.3:c.*645G>C	XP_006720445.1:n.*645G>C
NM_000743.5:c.*645G>C MANE Select	NP_000734.2:n.*645G>C
NM_001166694.2:c.1390-2768G>C	NP_001160166.1:n.1390-2768G>C
NR_046313.2:n.1784+581G>C