Canonical Allele Identifier: CA7684463

Gene: CHRNA3

Linked Data

• dbSNP Id: rs577413653
• ExAC: 15:78894483 C / T
• gnomAD v2: 15-78894483-C-T
• gnomAD v3: 15-78602141-C-T
• gnomAD v4: 15-78602141-C-T
• COSMIC: COSM1374802
• MyVariant Identifiers: chr15:g.78894483C>T (hg19) ; chr15:g.78602141C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602141C>T , CM000677.2:g.78602141C>T	GRCh38
NC_000015.9:g.78894483C>T , CM000677.1:g.78894483C>T	GRCh37
NC_000015.8:g.76681538C>T	NCBI36
NG_016143.1:g.24155G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.501G>A MANE Select	ENSP00000315602.5:p.Pro167=
ENST00000326828.5:c.501G>A	ENSP00000315602.5:p.Pro167=
ENST00000348639.7:c.501G>A	ENSP00000267951.4:p.Pro167=
ENST00000558903.1:n.208G>A
ENST00000559658.5:c.501G>A	ENSP00000452896.1:p.Pro167=
NM_000743.4:c.501G>A	NP_000734.2:p.Pro167=
NM_001166694.1:c.501G>A	NP_001160166.1:p.Pro167=
NR_046313.1:n.1002G>A
XM_006720382.1:c.300G>A	XP_006720445.1:p.Pro100=
XM_011521173.1:c.420G>A	XP_011519475.1:p.Pro140=
XM_006720382.3:c.300G>A	XP_006720445.1:p.Pro100=
NM_000743.5:c.501G>A MANE Select	NP_000734.2:p.Pro167=
NM_001166694.2:c.501G>A	NP_001160166.1:p.Pro167=
NR_046313.2:n.703G>A