Canonical Allele Identifier: CA273914148

Gene: CHRNA3

Linked Data

• dbSNP Id: rs976928051
• gnomAD v3: 15-78615626-T-C
• gnomAD v4: 15-78615626-T-C
• MyVariant Identifiers: chr15:g.78907968T>C (hg19) ; chr15:g.78615626T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78615626T>C , CM000677.2:g.78615626T>C	GRCh38
NC_000015.9:g.78907968T>C , CM000677.1:g.78907968T>C	GRCh37
NC_000015.8:g.76695023T>C	NCBI36
NG_016143.1:g.10670A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.377+1398A>G MANE Select	ENSP00000315602.5:n.377+1398A>G
ENST00000326828.5:c.377+1398A>G	ENSP00000315602.5:n.377+1398A>G
ENST00000348639.7:c.377+1398A>G	ENSP00000267951.4:n.377+1398A>G
ENST00000559658.5:c.377+1398A>G	ENSP00000452896.1:n.377+1398A>G
NM_000743.4:c.377+1398A>G	NP_000734.2:n.377+1398A>G
NM_001166694.1:c.377+1398A>G	NP_001160166.1:n.377+1398A>G
NR_046313.1:n.878+1398A>G
XM_006720382.1:c.176+1398A>G	XP_006720445.1:n.176+1398A>G
XM_011521173.1:c.296+1398A>G	XP_011519475.1:n.296+1398A>G
XM_006720382.3:c.176+1398A>G	XP_006720445.1:n.176+1398A>G
NM_000743.5:c.377+1398A>G MANE Select	NP_000734.2:n.377+1398A>G
NM_001166694.2:c.377+1398A>G	NP_001160166.1:n.377+1398A>G
NR_046313.2:n.579+1398A>G