Canonical Allele Identifier: CA2245822649

Gene: CHRNB1

Linked Data

• dbSNP Id: rs2069946507

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7455994C>G , CM000679.2:g.7455994C>G	GRCh38
NC_000017.10:g.7359313C>G , CM000679.1:g.7359313C>G	GRCh37
NC_000017.9:g.7300037C>G	NCBI36
NG_008026.1:g.15908C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306071.7:c.1365+53C>G MANE Select	ENSP00000304290.2:n.1365+53C>G
ENST00000306071.6:c.1365+53C>G	ENSP00000304290.2:n.1365+53C>G
ENST00000536404.6:c.1149+53C>G	ENSP00000439209.2:n.1149+53C>G
ENST00000575379.1:c.-28+53C>G	ENSP00000461751.1:n.-28+53C>G
ENST00000576360.1:c.1002+53C>G	ENSP00000459092.1:n.1002+53C>G
NM_000747.2:c.1365+53C>G	NP_000738.2:n.1365+53C>G
NM_000747.3:c.1365+53C>G MANE Select	NP_000738.2:n.1365+53C>G