Canonical Allele Identifier: CA7684535

Gene: CHRNA3

Linked Data

• dbSNP Id: rs77574318
• ExAC: 15:78909414 C / T
• gnomAD v2: 15-78909414-C-T
• gnomAD v3: 15-78617072-C-T
• gnomAD v4: 15-78617072-C-T
• MyVariant Identifiers: chr15:g.78909414C>T (hg19) ; chr15:g.78617072C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78617072C>T , CM000677.2:g.78617072C>T	GRCh38
NC_000015.9:g.78909414C>T , CM000677.1:g.78909414C>T	GRCh37
NC_000015.8:g.76696469C>T	NCBI36
NG_016143.1:g.9224G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.329G>A MANE Select	ENSP00000315602.5:p.Arg110His
ENST00000326828.5:c.329G>A	ENSP00000315602.5:p.Arg110His
ENST00000348639.7:c.329G>A	ENSP00000267951.4:p.Arg110His
ENST00000559658.5:c.329G>A	ENSP00000452896.1:p.Arg110His
NM_000743.4:c.329G>A	NP_000734.2:p.Arg110His
NM_001166694.1:c.329G>A	NP_001160166.1:p.Arg110His
NR_046313.1:n.830G>A
XM_006720382.1:c.128G>A	XP_006720445.1:p.Arg43His
XM_011521173.1:c.248G>A	XP_011519475.1:p.Arg83His
XM_006720382.3:c.128G>A	XP_006720445.1:p.Arg43His
NM_000743.5:c.329G>A MANE Select	NP_000734.2:p.Arg110His
NM_001166694.2:c.329G>A	NP_001160166.1:p.Arg110His
NR_046313.2:n.531G>A