Canonical Allele Identifier: CA2480925357

Gene: CHRNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571722A= , CM000663.2:g.154571722A=	GRCh38
NC_000001.10:g.154544198A= , CM000663.1:g.154544198A=	GRCh37
NC_000001.9:g.152810822A=	NCBI36
NG_008027.1:g.8942A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.899A= MANE Select	ENSP00000357461.3:p.Tyr300=
ENST00000636034.1:c.899A=	ENSP00000489703.1:p.Tyr300=
ENST00000637900.1:c.905A=	ENSP00000490474.1:p.Tyr302=
ENST00000368476.3:c.899A=	ENSP00000357461.3:p.Tyr300=
NM_000748.2:c.899A=	NP_000739.1:p.Tyr300=
XM_017000180.2:c.389A=	XP_016855669.1:p.Tyr130=
XR_001736952.2:n.1151A=
NM_000748.3:c.899A= MANE Select	NP_000739.1:p.Tyr300=