Canonical Allele Identifier: CA2629789470

Gene: CHRNA3

Linked Data

• gnomAD v4: 15-78602365-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602365G>T , CM000677.2:g.78602365G>T	GRCh38
NC_000015.9:g.78894707G>T , CM000677.1:g.78894707G>T	GRCh37
NC_000015.8:g.76681762G>T	NCBI36
NG_016143.1:g.23931C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.378-101C>A MANE Select	ENSP00000315602.5:n.378-101C>A
ENST00000326828.5:c.378-101C>A	ENSP00000315602.5:n.378-101C>A
ENST00000348639.7:c.378-101C>A	ENSP00000267951.4:n.378-101C>A
ENST00000558903.1:n.85-101C>A
ENST00000559658.5:c.378-101C>A	ENSP00000452896.1:n.378-101C>A
NM_000743.4:c.378-101C>A	NP_000734.2:n.378-101C>A
NM_001166694.1:c.378-101C>A	NP_001160166.1:n.378-101C>A
NR_046313.1:n.879-101C>A
XM_006720382.1:c.177-101C>A	XP_006720445.1:n.177-101C>A
XM_011521173.1:c.297-101C>A	XP_011519475.1:n.297-101C>A
XM_006720382.3:c.177-101C>A	XP_006720445.1:n.177-101C>A
NM_000743.5:c.378-101C>A MANE Select	NP_000734.2:n.378-101C>A
NM_001166694.2:c.378-101C>A	NP_001160166.1:n.378-101C>A
NR_046313.2:n.580-101C>A