Canonical Allele Identifier: CA273900176

Gene: CHRNA3

Linked Data

• dbSNP Id: rs146990002
• gnomAD v2: 15-78888209-T-C
• gnomAD v3: 15-78595867-T-C
• gnomAD v4: 15-78595867-T-C
• MyVariant Identifiers: chr15:g.78888209T>C (hg19) ; chr15:g.78595867T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78595867T>C , CM000677.2:g.78595867T>C	GRCh38
NC_000015.9:g.78888209T>C , CM000677.1:g.78888209T>C	GRCh37
NC_000015.8:g.76675264T>C	NCBI36
NG_016143.1:g.30429A>G
NG_023328.1:g.35348T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.*737A>G MANE Select	ENSP00000315602.5:n.*737A>G
ENST00000326828.5:c.*737A>G	ENSP00000315602.5:n.*737A>G
ENST00000348639.7:c.1390-2676A>G	ENSP00000267951.4:n.1390-2676A>G
ENST00000559002.5:n.193+673A>G
ENST00000559658.5:c.*64+673A>G	ENSP00000452896.1:n.*64+673A>G
NM_000743.4:c.*737A>G	NP_000734.2:n.*737A>G
NM_001166694.1:c.1390-2676A>G	NP_001160166.1:n.1390-2676A>G
NR_046313.1:n.2083+673A>G
XM_006720382.1:c.*737A>G	XP_006720445.1:n.*737A>G
XM_011521173.1:c.*737A>G	XP_011519475.1:n.*737A>G
XM_006720382.3:c.*737A>G	XP_006720445.1:n.*737A>G
NM_000743.5:c.*737A>G MANE Select	NP_000734.2:n.*737A>G
NM_001166694.2:c.1390-2676A>G	NP_001160166.1:n.1390-2676A>G
NR_046313.2:n.1784+673A>G