Canonical Allele Identifier: CA420970248

Gene: CHRNB2

Linked Data

• MyVariant Identifiers: chr1:g.154543668T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571192T>G , CM000663.2:g.154571192T>G	GRCh38
NC_000001.10:g.154543668T>G , CM000663.1:g.154543668T>G	GRCh37
NC_000001.9:g.152810292T>G	NCBI36
NG_008027.1:g.8412T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.369T>G MANE Select	ENSP00000357461.3:p.Ala123=
ENST00000636034.1:c.369T>G	ENSP00000489703.1:p.Ala123=
ENST00000637900.1:c.375T>G	ENSP00000490474.1:p.Ala125=
ENST00000368476.3:c.369T>G	ENSP00000357461.3:p.Ala123=
NM_000748.2:c.369T>G	NP_000739.1:p.Ala123=
XM_017000180.2:c.-9-133T>G	XP_016855669.1:n.-9-133T>G
XR_001736952.2:n.621T>G
NM_000748.3:c.369T>G MANE Select	NP_000739.1:p.Ala123=