Canonical Allele Identifier: CA497744708

Gene: CHRNB1

Linked Data

• MyVariant Identifiers: chr17:g.7357803A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7454484A>G , CM000679.2:g.7454484A>G	GRCh38
NC_000017.10:g.7357803A>G , CM000679.1:g.7357803A>G	GRCh37
NC_000017.9:g.7298527A>G	NCBI36
NG_008026.1:g.14398A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306071.7:c.1008A>G MANE Select	ENSP00000304290.2:p.Ser336=
ENST00000306071.6:c.1008A>G	ENSP00000304290.2:p.Ser336=
ENST00000536404.6:c.792A>G	ENSP00000439209.2:p.Ser264=
ENST00000570557.5:c.671A>G
ENST00000573209.1:n.1952A>G
ENST00000576360.1:c.645A>G	ENSP00000459092.1:p.Ser215=
NM_000747.2:c.1008A>G	NP_000738.2:p.Ser336=
NM_000747.3:c.1008A>G MANE Select	NP_000738.2:p.Ser336=