Canonical Allele Identifier: CA273906149

Gene: CHRNA3

Linked Data

• dbSNP Id: rs986989522
• gnomAD v4: 15-78602381-A-G
• MyVariant Identifiers: chr15:g.78894723A>G (hg19) ; chr15:g.78602381A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602381A>G , CM000677.2:g.78602381A>G	GRCh38
NC_000015.9:g.78894723A>G , CM000677.1:g.78894723A>G	GRCh37
NC_000015.8:g.76681778A>G	NCBI36
NG_016143.1:g.23915T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.378-117T>C MANE Select	ENSP00000315602.5:n.378-117T>C
ENST00000326828.5:c.378-117T>C	ENSP00000315602.5:n.378-117T>C
ENST00000348639.7:c.378-117T>C	ENSP00000267951.4:n.378-117T>C
ENST00000558903.1:n.85-117T>C
ENST00000559658.5:c.378-117T>C	ENSP00000452896.1:n.378-117T>C
NM_000743.4:c.378-117T>C	NP_000734.2:n.378-117T>C
NM_001166694.1:c.378-117T>C	NP_001160166.1:n.378-117T>C
NR_046313.1:n.879-117T>C
XM_006720382.1:c.177-117T>C	XP_006720445.1:n.177-117T>C
XM_011521173.1:c.297-117T>C	XP_011519475.1:n.297-117T>C
XM_006720382.3:c.177-117T>C	XP_006720445.1:n.177-117T>C
NM_000743.5:c.378-117T>C MANE Select	NP_000734.2:n.378-117T>C
NM_001166694.2:c.378-117T>C	NP_001160166.1:n.378-117T>C
NR_046313.2:n.580-117T>C