Canonical Allele Identifier: CA491620987

Gene: CHRNA3

Linked Data

• MyVariant Identifiers: chr15:g.78911190G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78618848G>A , CM000677.2:g.78618848G>A	GRCh38
NC_000015.9:g.78911190G>A , CM000677.1:g.78911190G>A	GRCh37
NC_000015.8:g.76698245G>A	NCBI36
NG_016143.1:g.7448C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.150C>T MANE Select	ENSP00000315602.5:p.Ile50=
ENST00000326828.5:c.150C>T	ENSP00000315602.5:p.Ile50=
ENST00000348639.7:c.150C>T	ENSP00000267951.4:p.Ile50=
ENST00000559080.1:c.-52C>T	ENSP00000453993.1:n.-52C>T
ENST00000559658.5:c.150C>T	ENSP00000452896.1:p.Ile50=
ENST00000561128.1:n.145C>T
NM_000743.4:c.150C>T	NP_000734.2:p.Ile50=
NM_001166694.1:c.150C>T	NP_001160166.1:p.Ile50=
NR_046313.1:n.651C>T
XM_006720382.1:c.-52C>T	XP_006720445.1:n.-52C>T
XM_011521173.1:c.69C>T	XP_011519475.1:p.Ile23=
XM_006720382.3:c.-52C>T	XP_006720445.1:n.-52C>T
NM_000743.5:c.150C>T MANE Select	NP_000734.2:p.Ile50=
NM_001166694.2:c.150C>T	NP_001160166.1:p.Ile50=
NR_046313.2:n.352C>T