Canonical Allele Identifier: CA393576204

Gene: CHRNA3

Linked Data

• MyVariant Identifiers: chr15:g.78911183C>G (hg19) ; chr15:g.78618841C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78618841C>G , CM000677.2:g.78618841C>G	GRCh38
NC_000015.9:g.78911183C>G , CM000677.1:g.78911183C>G	GRCh37
NC_000015.8:g.76698238C>G	NCBI36
NG_016143.1:g.7455G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.157G>C MANE Select	ENSP00000315602.5:p.Val53Leu
ENST00000326828.5:c.157G>C	ENSP00000315602.5:p.Val53Leu
ENST00000348639.7:c.157G>C	ENSP00000267951.4:p.Val53Leu
ENST00000559080.1:c.-45G>C	ENSP00000453993.1:n.-45G>C
ENST00000559658.5:c.157G>C	ENSP00000452896.1:p.Val53Leu
ENST00000561128.1:n.152G>C
NM_000743.4:c.157G>C	NP_000734.2:p.Val53Leu
NM_001166694.1:c.157G>C	NP_001160166.1:p.Val53Leu
NR_046313.1:n.658G>C
XM_006720382.1:c.-45G>C	XP_006720445.1:n.-45G>C
XM_011521173.1:c.76G>C	XP_011519475.1:p.Val26Leu
XM_006720382.3:c.-45G>C	XP_006720445.1:n.-45G>C
NM_000743.5:c.157G>C MANE Select	NP_000734.2:p.Val53Leu
NM_001166694.2:c.157G>C	NP_001160166.1:p.Val53Leu
NR_046313.2:n.359G>C