Canonical Allele Identifier: CA971789591

Gene: CHRNA3

Linked Data

• dbSNP Id: rs2053471341
• gnomAD v3: 15-78616949-T-A
• gnomAD v4: 15-78616949-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78616949T>A , CM000677.2:g.78616949T>A	GRCh38
NC_000015.9:g.78909291T>A , CM000677.1:g.78909291T>A	GRCh37
NC_000015.8:g.76696346T>A	NCBI36
NG_016143.1:g.9347A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.377+75A>T MANE Select	ENSP00000315602.5:n.377+75A>T
ENST00000326828.5:c.377+75A>T	ENSP00000315602.5:n.377+75A>T
ENST00000348639.7:c.377+75A>T	ENSP00000267951.4:n.377+75A>T
ENST00000559658.5:c.377+75A>T	ENSP00000452896.1:n.377+75A>T
NM_000743.4:c.377+75A>T	NP_000734.2:n.377+75A>T
NM_001166694.1:c.377+75A>T	NP_001160166.1:n.377+75A>T
NR_046313.1:n.878+75A>T
XM_006720382.1:c.176+75A>T	XP_006720445.1:n.176+75A>T
XM_011521173.1:c.296+75A>T	XP_011519475.1:n.296+75A>T
XM_006720382.3:c.176+75A>T	XP_006720445.1:n.176+75A>T
NM_000743.5:c.377+75A>T MANE Select	NP_000734.2:n.377+75A>T
NM_001166694.2:c.377+75A>T	NP_001160166.1:n.377+75A>T
NR_046313.2:n.579+75A>T