Canonical Allele Identifier: CA7684533

Gene: CHRNA3

Linked Data

• dbSNP Id: rs776712876
• ExAC: 15:78909407 A / G
• gnomAD v2: 15-78909407-A-G
• gnomAD v4: 15-78617065-A-G
• MyVariant Identifiers: chr15:g.78909407A>G (hg19) ; chr15:g.78617065A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78617065A>G , CM000677.2:g.78617065A>G	GRCh38
NC_000015.9:g.78909407A>G , CM000677.1:g.78909407A>G	GRCh37
NC_000015.8:g.76696462A>G	NCBI36
NG_016143.1:g.9231T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.336T>C MANE Select	ENSP00000315602.5:p.Pro112=
ENST00000326828.5:c.336T>C	ENSP00000315602.5:p.Pro112=
ENST00000348639.7:c.336T>C	ENSP00000267951.4:p.Pro112=
ENST00000559658.5:c.336T>C	ENSP00000452896.1:p.Pro112=
NM_000743.4:c.336T>C	NP_000734.2:p.Pro112=
NM_001166694.1:c.336T>C	NP_001160166.1:p.Pro112=
NR_046313.1:n.837T>C
XM_006720382.1:c.135T>C	XP_006720445.1:p.Pro45=
XM_011521173.1:c.255T>C	XP_011519475.1:p.Pro85=
XM_006720382.3:c.135T>C	XP_006720445.1:p.Pro45=
NM_000743.5:c.336T>C MANE Select	NP_000734.2:p.Pro112=
NM_001166694.2:c.336T>C	NP_001160166.1:p.Pro112=
NR_046313.2:n.538T>C