Canonical Allele Identifier: CA7684395

Gene: CHRNA3

Linked Data

• dbSNP Id: rs368009411
• ExAC: 15:78894147 G / A
• gnomAD v2: 15-78894147-G-A
• gnomAD v3: 15-78601805-G-A
• gnomAD v4: 15-78601805-G-A
• MyVariant Identifiers: chr15:g.78894147G>A (hg19) ; chr15:g.78601805G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601805G>A , CM000677.2:g.78601805G>A	GRCh38
NC_000015.9:g.78894147G>A , CM000677.1:g.78894147G>A	GRCh37
NC_000015.8:g.76681202G>A	NCBI36
NG_016143.1:g.24491C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.837C>T MANE Select	ENSP00000315602.5:p.Val279=
ENST00000326828.5:c.837C>T	ENSP00000315602.5:p.Val279=
ENST00000348639.7:c.837C>T	ENSP00000267951.4:p.Val279=
ENST00000558903.1:n.544C>T
ENST00000559658.5:c.837C>T	ENSP00000452896.1:p.Val279=
NM_000743.4:c.837C>T	NP_000734.2:p.Val279=
NM_001166694.1:c.837C>T	NP_001160166.1:p.Val279=
NR_046313.1:n.1338C>T
XM_006720382.1:c.636C>T	XP_006720445.1:p.Val212=
XM_011521173.1:c.756C>T	XP_011519475.1:p.Val252=
XM_006720382.3:c.636C>T	XP_006720445.1:p.Val212=
NM_000743.5:c.837C>T MANE Select	NP_000734.2:p.Val279=
NM_001166694.2:c.837C>T	NP_001160166.1:p.Val279=
NR_046313.2:n.1039C>T