Canonical Allele Identifier: CA393576208

Gene: CHRNA3

Linked Data

• MyVariant Identifiers: chr15:g.78911185G>C (hg19) ; chr15:g.78618843G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78618843G>C , CM000677.2:g.78618843G>C	GRCh38
NC_000015.9:g.78911185G>C , CM000677.1:g.78911185G>C	GRCh37
NC_000015.8:g.76698240G>C	NCBI36
NG_016143.1:g.7453C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.155C>G MANE Select	ENSP00000315602.5:p.Pro52Arg
ENST00000326828.5:c.155C>G	ENSP00000315602.5:p.Pro52Arg
ENST00000348639.7:c.155C>G	ENSP00000267951.4:p.Pro52Arg
ENST00000559080.1:c.-47C>G	ENSP00000453993.1:n.-47C>G
ENST00000559658.5:c.155C>G	ENSP00000452896.1:p.Pro52Arg
ENST00000561128.1:n.150C>G
NM_000743.4:c.155C>G	NP_000734.2:p.Pro52Arg
NM_001166694.1:c.155C>G	NP_001160166.1:p.Pro52Arg
NR_046313.1:n.656C>G
XM_006720382.1:c.-47C>G	XP_006720445.1:n.-47C>G
XM_011521173.1:c.74C>G	XP_011519475.1:p.Pro25Arg
XM_006720382.3:c.-47C>G	XP_006720445.1:n.-47C>G
NM_000743.5:c.155C>G MANE Select	NP_000734.2:p.Pro52Arg
NM_001166694.2:c.155C>G	NP_001160166.1:p.Pro52Arg
NR_046313.2:n.357C>G