Canonical Allele Identifier: CA273915183

Gene: CHRNA3

Linked Data

• dbSNP Id: rs267604333
• MyVariant Identifiers: chr15:g.78909403G>A (hg19) ; chr15:g.78617061G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78617061G>A , CM000677.2:g.78617061G>A	GRCh38
NC_000015.9:g.78909403G>A , CM000677.1:g.78909403G>A	GRCh37
NC_000015.8:g.76696458G>A	NCBI36
NG_016143.1:g.9235C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.340C>T MANE Select	ENSP00000315602.5:p.Gln114Ter
ENST00000326828.5:c.340C>T	ENSP00000315602.5:p.Gln114Ter
ENST00000348639.7:c.340C>T	ENSP00000267951.4:p.Gln114Ter
ENST00000559658.5:c.340C>T	ENSP00000452896.1:p.Gln114Ter
NM_000743.4:c.340C>T	NP_000734.2:p.Gln114Ter
NM_001166694.1:c.340C>T	NP_001160166.1:p.Gln114Ter
NR_046313.1:n.841C>T
XM_006720382.1:c.139C>T	XP_006720445.1:p.Gln47Ter
XM_011521173.1:c.259C>T	XP_011519475.1:p.Gln87Ter
XM_006720382.3:c.139C>T	XP_006720445.1:p.Gln47Ter
NM_000743.5:c.340C>T MANE Select	NP_000734.2:p.Gln114Ter
NM_001166694.2:c.340C>T	NP_001160166.1:p.Gln114Ter
NR_046313.2:n.542C>T