Canonical Allele Identifier: CA971789308

Gene: CHRNA3

Linked Data

• dbSNP Id: rs2053448542
• gnomAD v3: 15-78615563-A-T
• gnomAD v4: 15-78615563-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78615563A>T , CM000677.2:g.78615563A>T	GRCh38
NC_000015.9:g.78907905A>T , CM000677.1:g.78907905A>T	GRCh37
NC_000015.8:g.76694960A>T	NCBI36
NG_016143.1:g.10733T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.377+1461T>A MANE Select	ENSP00000315602.5:n.377+1461T>A
ENST00000326828.5:c.377+1461T>A	ENSP00000315602.5:n.377+1461T>A
ENST00000348639.7:c.377+1461T>A	ENSP00000267951.4:n.377+1461T>A
ENST00000559658.5:c.377+1461T>A	ENSP00000452896.1:n.377+1461T>A
NM_000743.4:c.377+1461T>A	NP_000734.2:n.377+1461T>A
NM_001166694.1:c.377+1461T>A	NP_001160166.1:n.377+1461T>A
NR_046313.1:n.878+1461T>A
XM_006720382.1:c.176+1461T>A	XP_006720445.1:n.176+1461T>A
XM_011521173.1:c.296+1461T>A	XP_011519475.1:n.296+1461T>A
XM_006720382.3:c.176+1461T>A	XP_006720445.1:n.176+1461T>A
NM_000743.5:c.377+1461T>A MANE Select	NP_000734.2:n.377+1461T>A
NM_001166694.2:c.377+1461T>A	NP_001160166.1:n.377+1461T>A
NR_046313.2:n.579+1461T>A