Canonical Allele Identifier: CA393585022

Gene: CHRNA3

Linked Data

• MyVariant Identifiers: chr15:g.78894258C>G (hg19) ; chr15:g.78601916C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601916C>G , CM000677.2:g.78601916C>G	GRCh38
NC_000015.9:g.78894258C>G , CM000677.1:g.78894258C>G	GRCh37
NC_000015.8:g.76681313C>G	NCBI36
NG_016143.1:g.24380G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.726G>C MANE Select	ENSP00000315602.5:p.Leu242Phe
ENST00000326828.5:c.726G>C	ENSP00000315602.5:p.Leu242Phe
ENST00000348639.7:c.726G>C	ENSP00000267951.4:p.Leu242Phe
ENST00000558903.1:n.433G>C
ENST00000559658.5:c.726G>C	ENSP00000452896.1:p.Leu242Phe
NM_000743.4:c.726G>C	NP_000734.2:p.Leu242Phe
NM_001166694.1:c.726G>C	NP_001160166.1:p.Leu242Phe
NR_046313.1:n.1227G>C
XM_006720382.1:c.525G>C	XP_006720445.1:p.Leu175Phe
XM_011521173.1:c.645G>C	XP_011519475.1:p.Leu215Phe
XM_006720382.3:c.525G>C	XP_006720445.1:p.Leu175Phe
NM_000743.5:c.726G>C MANE Select	NP_000734.2:p.Leu242Phe
NM_001166694.2:c.726G>C	NP_001160166.1:p.Leu242Phe
NR_046313.2:n.928G>C