Canonical Allele Identifier: CA491986521

Gene: CHRNA3

Linked Data

• MyVariant Identifiers: chr15:g.78894543C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602201C>G , CM000677.2:g.78602201C>G	GRCh38
NC_000015.9:g.78894543C>G , CM000677.1:g.78894543C>G	GRCh37
NC_000015.8:g.76681598C>G	NCBI36
NG_016143.1:g.24095G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.441G>C MANE Select	ENSP00000315602.5:p.Val147=
ENST00000326828.5:c.441G>C	ENSP00000315602.5:p.Val147=
ENST00000348639.7:c.441G>C	ENSP00000267951.4:p.Val147=
ENST00000558903.1:n.148G>C
ENST00000559658.5:c.441G>C	ENSP00000452896.1:p.Val147=
NM_000743.4:c.441G>C	NP_000734.2:p.Val147=
NM_001166694.1:c.441G>C	NP_001160166.1:p.Val147=
NR_046313.1:n.942G>C
XM_006720382.1:c.240G>C	XP_006720445.1:p.Val80=
XM_011521173.1:c.360G>C	XP_011519475.1:p.Val120=
XM_006720382.3:c.240G>C	XP_006720445.1:p.Val80=
NM_000743.5:c.441G>C MANE Select	NP_000734.2:p.Val147=
NM_001166694.2:c.441G>C	NP_001160166.1:p.Val147=
NR_046313.2:n.643G>C