Canonical Allele Identifier: CA7684620

Gene: CHRNA3

Linked Data

• ClinVar Variation Id: 2402975
• ClinVar RCV Id: RCV002783940
• dbSNP Id: rs765428894
• ExAC: 15:78911189 G / A
• gnomAD v2: 15-78911189-G-A
• gnomAD v3: 15-78618847-G-A
• gnomAD v4: 15-78618847-G-A
• MyVariant Identifiers: chr15:g.78911189G>A (hg19) ; chr15:g.78618847G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78618847G>A , CM000677.2:g.78618847G>A	GRCh38
NC_000015.9:g.78911189G>A , CM000677.1:g.78911189G>A	GRCh37
NC_000015.8:g.76698244G>A	NCBI36
NG_016143.1:g.7449C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.151C>T MANE Select	ENSP00000315602.5:p.Arg51Trp
ENST00000326828.5:c.151C>T	ENSP00000315602.5:p.Arg51Trp
ENST00000348639.7:c.151C>T	ENSP00000267951.4:p.Arg51Trp
ENST00000559080.1:c.-51C>T	ENSP00000453993.1:n.-51C>T
ENST00000559658.5:c.151C>T	ENSP00000452896.1:p.Arg51Trp
ENST00000561128.1:n.146C>T
NM_000743.4:c.151C>T	NP_000734.2:p.Arg51Trp
NM_001166694.1:c.151C>T	NP_001160166.1:p.Arg51Trp
NR_046313.1:n.652C>T
XM_006720382.1:c.-51C>T	XP_006720445.1:n.-51C>T
XM_011521173.1:c.70C>T	XP_011519475.1:p.Arg24Trp
XM_006720382.3:c.-51C>T	XP_006720445.1:n.-51C>T
NM_000743.5:c.151C>T MANE Select	NP_000734.2:p.Arg51Trp
NM_001166694.2:c.151C>T	NP_001160166.1:p.Arg51Trp
NR_046313.2:n.353C>T