Canonical Allele Identifier: CA497745006

Gene: CHRNB1

Linked Data

• MyVariant Identifiers: chr17:g.7359197G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7455878G>T , CM000679.2:g.7455878G>T	GRCh38
NC_000017.10:g.7359197G>T , CM000679.1:g.7359197G>T	GRCh37
NC_000017.9:g.7299921G>T	NCBI36
NG_008026.1:g.15792G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306071.7:c.1302G>T MANE Select	ENSP00000304290.2:p.Arg434=
ENST00000306071.6:c.1302G>T	ENSP00000304290.2:p.Arg434=
ENST00000536404.6:c.1086G>T	ENSP00000439209.2:p.Arg362=
ENST00000575379.1:c.-91G>T	ENSP00000461751.1:n.-91G>T
ENST00000576360.1:c.939G>T	ENSP00000459092.1:p.Arg313=
NM_000747.2:c.1302G>T	NP_000738.2:p.Arg434=
NM_000747.3:c.1302G>T MANE Select	NP_000738.2:p.Arg434=