Canonical Allele Identifier: CA393589049

Gene: CHRNA3

Linked Data

• dbSNP Id: rs972546811
• MyVariant Identifiers: chr15:g.78909409G>A (hg19) ; chr15:g.78617067G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78617067G>A , CM000677.2:g.78617067G>A	GRCh38
NC_000015.9:g.78909409G>A , CM000677.1:g.78909409G>A	GRCh37
NC_000015.8:g.76696464G>A	NCBI36
NG_016143.1:g.9229C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.334C>T MANE Select	ENSP00000315602.5:p.Pro112Ser
ENST00000326828.5:c.334C>T	ENSP00000315602.5:p.Pro112Ser
ENST00000348639.7:c.334C>T	ENSP00000267951.4:p.Pro112Ser
ENST00000559658.5:c.334C>T	ENSP00000452896.1:p.Pro112Ser
NM_000743.4:c.334C>T	NP_000734.2:p.Pro112Ser
NM_001166694.1:c.334C>T	NP_001160166.1:p.Pro112Ser
NR_046313.1:n.835C>T
XM_006720382.1:c.133C>T	XP_006720445.1:p.Pro45Ser
XM_011521173.1:c.253C>T	XP_011519475.1:p.Pro85Ser
XM_006720382.3:c.133C>T	XP_006720445.1:p.Pro45Ser
NM_000743.5:c.334C>T MANE Select	NP_000734.2:p.Pro112Ser
NM_001166694.2:c.334C>T	NP_001160166.1:p.Pro112Ser
NR_046313.2:n.536C>T