Canonical Allele Identifier: CA7684616

Gene: CHRNA3

Linked Data

• dbSNP Id: rs754431447
• ExAC: 15:78911182 A / G
• gnomAD v4: 15-78618840-A-G
• MyVariant Identifiers: chr15:g.78911182A>G (hg19) ; chr15:g.78618840A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78618840A>G , CM000677.2:g.78618840A>G	GRCh38
NC_000015.9:g.78911182A>G , CM000677.1:g.78911182A>G	GRCh37
NC_000015.8:g.76698237A>G	NCBI36
NG_016143.1:g.7456T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.158T>C MANE Select	ENSP00000315602.5:p.Val53Ala
ENST00000326828.5:c.158T>C	ENSP00000315602.5:p.Val53Ala
ENST00000348639.7:c.158T>C	ENSP00000267951.4:p.Val53Ala
ENST00000559080.1:c.-44T>C	ENSP00000453993.1:n.-44T>C
ENST00000559658.5:c.158T>C	ENSP00000452896.1:p.Val53Ala
ENST00000561128.1:n.153T>C
NM_000743.4:c.158T>C	NP_000734.2:p.Val53Ala
NM_001166694.1:c.158T>C	NP_001160166.1:p.Val53Ala
NR_046313.1:n.659T>C
XM_006720382.1:c.-44T>C	XP_006720445.1:n.-44T>C
XM_011521173.1:c.77T>C	XP_011519475.1:p.Val26Ala
XM_006720382.3:c.-44T>C	XP_006720445.1:n.-44T>C
NM_000743.5:c.158T>C MANE Select	NP_000734.2:p.Val53Ala
NM_001166694.2:c.158T>C	NP_001160166.1:p.Val53Ala
NR_046313.2:n.360T>C