Canonical Allele Identifier: CA397802624

Gene: CHRNB1

Linked Data

• MyVariant Identifiers: chr17:g.7359200G>T (hg19) ; chr17:g.7455881G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7455881G>T , CM000679.2:g.7455881G>T	GRCh38
NC_000017.10:g.7359200G>T , CM000679.1:g.7359200G>T	GRCh37
NC_000017.9:g.7299924G>T	NCBI36
NG_008026.1:g.15795G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000306071.7:c.1305G>T MANE Select	ENSP00000304290.2:p.Glu435Asp
ENST00000306071.6:c.1305G>T	ENSP00000304290.2:p.Glu435Asp
ENST00000536404.6:c.1089G>T	ENSP00000439209.2:p.Glu363Asp
ENST00000575379.1:c.-88G>T	ENSP00000461751.1:n.-88G>T
ENST00000576360.1:c.942G>T	ENSP00000459092.1:p.Glu314Asp
NM_000747.2:c.1305G>T	NP_000738.2:p.Glu435Asp
NM_000747.3:c.1305G>T MANE Select	NP_000738.2:p.Glu435Asp