Canonical Allele Identifier: CA393576212

Gene: CHRNA3

Linked Data

• MyVariant Identifiers: chr15:g.78911188C>A (hg19) ; chr15:g.78618846C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78618846C>A , CM000677.2:g.78618846C>A	GRCh38
NC_000015.9:g.78911188C>A , CM000677.1:g.78911188C>A	GRCh37
NC_000015.8:g.76698243C>A	NCBI36
NG_016143.1:g.7450G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.152G>T MANE Select	ENSP00000315602.5:p.Arg51Leu
ENST00000326828.5:c.152G>T	ENSP00000315602.5:p.Arg51Leu
ENST00000348639.7:c.152G>T	ENSP00000267951.4:p.Arg51Leu
ENST00000559080.1:c.-50G>T	ENSP00000453993.1:n.-50G>T
ENST00000559658.5:c.152G>T	ENSP00000452896.1:p.Arg51Leu
ENST00000561128.1:n.147G>T
NM_000743.4:c.152G>T	NP_000734.2:p.Arg51Leu
NM_001166694.1:c.152G>T	NP_001160166.1:p.Arg51Leu
NR_046313.1:n.653G>T
XM_006720382.1:c.-50G>T	XP_006720445.1:n.-50G>T
XM_011521173.1:c.71G>T	XP_011519475.1:p.Arg24Leu
XM_006720382.3:c.-50G>T	XP_006720445.1:n.-50G>T
NM_000743.5:c.152G>T MANE Select	NP_000734.2:p.Arg51Leu
NM_001166694.2:c.152G>T	NP_001160166.1:p.Arg51Leu
NR_046313.2:n.354G>T