Canonical Allele Identifier: CA273906116

Gene: CHRNA3

Linked Data

• dbSNP Id: rs74877920
• gnomAD v2: 15-78894688-A-C
• gnomAD v3: 15-78602346-A-C
• gnomAD v4: 15-78602346-A-C
• MyVariant Identifiers: chr15:g.78894688A>C (hg19) ; chr15:g.78602346A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602346A>C , CM000677.2:g.78602346A>C	GRCh38
NC_000015.9:g.78894688A>C , CM000677.1:g.78894688A>C	GRCh37
NC_000015.8:g.76681743A>C	NCBI36
NG_016143.1:g.23950T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.378-82T>G MANE Select	ENSP00000315602.5:n.378-82T>G
ENST00000326828.5:c.378-82T>G	ENSP00000315602.5:n.378-82T>G
ENST00000348639.7:c.378-82T>G	ENSP00000267951.4:n.378-82T>G
ENST00000558903.1:n.85-82T>G
ENST00000559658.5:c.378-82T>G	ENSP00000452896.1:n.378-82T>G
NM_000743.4:c.378-82T>G	NP_000734.2:n.378-82T>G
NM_001166694.1:c.378-82T>G	NP_001160166.1:n.378-82T>G
NR_046313.1:n.879-82T>G
XM_006720382.1:c.177-82T>G	XP_006720445.1:n.177-82T>G
XM_011521173.1:c.297-82T>G	XP_011519475.1:n.297-82T>G
XM_006720382.3:c.177-82T>G	XP_006720445.1:n.177-82T>G
NM_000743.5:c.378-82T>G MANE Select	NP_000734.2:n.378-82T>G
NM_001166694.2:c.378-82T>G	NP_001160166.1:n.378-82T>G
NR_046313.2:n.580-82T>G