Canonical Allele Identifier: CA2635846697

Gene: CHRNB1

Linked Data

• gnomAD v4: 17-7455763-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7455763G>T , CM000679.2:g.7455763G>T	GRCh38
NC_000017.10:g.7359082G>T , CM000679.1:g.7359082G>T	GRCh37
NC_000017.9:g.7299806G>T	NCBI36
NG_008026.1:g.15677G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306071.7:c.1218-31G>T MANE Select	ENSP00000304290.2:n.1218-31G>T
ENST00000306071.6:c.1218-31G>T	ENSP00000304290.2:n.1218-31G>T
ENST00000536404.6:c.1002-31G>T	ENSP00000439209.2:n.1002-31G>T
ENST00000570557.5:c.881-31G>T
ENST00000575379.1:c.-206G>T	ENSP00000461751.1:n.-206G>T
ENST00000576360.1:c.855-31G>T	ENSP00000459092.1:n.855-31G>T
NM_000747.2:c.1218-31G>T	NP_000738.2:n.1218-31G>T
NM_000747.3:c.1218-31G>T MANE Select	NP_000738.2:n.1218-31G>T