Canonical Allele Identifier: CA491986584

Gene: CHRNA3

Linked Data

• dbSNP Id: rs79106783
• gnomAD v2: 15-78894282-C-G
• gnomAD v4: 15-78601940-C-G
• MyVariant Identifiers: chr15:g.78894282C>G (hg19) ; chr15:g.78601940C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601940C>G , CM000677.2:g.78601940C>G	GRCh38
NC_000015.9:g.78894282C>G , CM000677.1:g.78894282C>G	GRCh37
NC_000015.8:g.76681337C>G	NCBI36
NG_016143.1:g.24356G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.702G>C MANE Select	ENSP00000315602.5:p.Ser234=
ENST00000326828.5:c.702G>C	ENSP00000315602.5:p.Ser234=
ENST00000348639.7:c.702G>C	ENSP00000267951.4:p.Ser234=
ENST00000558903.1:n.409G>C
ENST00000559658.5:c.702G>C	ENSP00000452896.1:p.Ser234=
NM_000743.4:c.702G>C	NP_000734.2:p.Ser234=
NM_001166694.1:c.702G>C	NP_001160166.1:p.Ser234=
NR_046313.1:n.1203G>C
XM_006720382.1:c.501G>C	XP_006720445.1:p.Ser167=
XM_011521173.1:c.621G>C	XP_011519475.1:p.Ser207=
XM_006720382.3:c.501G>C	XP_006720445.1:p.Ser167=
NM_000743.5:c.702G>C MANE Select	NP_000734.2:p.Ser234=
NM_001166694.2:c.702G>C	NP_001160166.1:p.Ser234=
NR_046313.2:n.904G>C