Canonical Allele Identifier: CA491620980

Gene: CHRNA3

Linked Data

• MyVariant Identifiers: chr15:g.78911184A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78618842A>C , CM000677.2:g.78618842A>C	GRCh38
NC_000015.9:g.78911184A>C , CM000677.1:g.78911184A>C	GRCh37
NC_000015.8:g.76698239A>C	NCBI36
NG_016143.1:g.7454T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.156T>G MANE Select	ENSP00000315602.5:p.Pro52=
ENST00000326828.5:c.156T>G	ENSP00000315602.5:p.Pro52=
ENST00000348639.7:c.156T>G	ENSP00000267951.4:p.Pro52=
ENST00000559080.1:c.-46T>G	ENSP00000453993.1:n.-46T>G
ENST00000559658.5:c.156T>G	ENSP00000452896.1:p.Pro52=
ENST00000561128.1:n.151T>G
NM_000743.4:c.156T>G	NP_000734.2:p.Pro52=
NM_001166694.1:c.156T>G	NP_001160166.1:p.Pro52=
NR_046313.1:n.657T>G
XM_006720382.1:c.-46T>G	XP_006720445.1:n.-46T>G
XM_011521173.1:c.75T>G	XP_011519475.1:p.Pro25=
XM_006720382.3:c.-46T>G	XP_006720445.1:n.-46T>G
NM_000743.5:c.156T>G MANE Select	NP_000734.2:p.Pro52=
NM_001166694.2:c.156T>G	NP_001160166.1:p.Pro52=
NR_046313.2:n.358T>G