Canonical Allele Identifier: CA1141761858

Gene: CHRNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571648G= , CM000663.2:g.154571648G=	GRCh38
NC_000001.10:g.154544124G= , CM000663.1:g.154544124G=	GRCh37
NC_000001.9:g.152810748G=	NCBI36
NG_008027.1:g.8868G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.825G= MANE Select	ENSP00000357461.3:p.Ala275=
ENST00000636034.1:c.825G=	ENSP00000489703.1:p.Ala275=
ENST00000637900.1:c.831G=	ENSP00000490474.1:p.Ala277=
ENST00000368476.3:c.825G=	ENSP00000357461.3:p.Ala275=
NM_000748.2:c.825G=	NP_000739.1:p.Ala275=
XM_017000180.2:c.315G=	XP_016855669.1:p.Ala105=
XR_001736952.2:n.1077G=
NM_000748.3:c.825G= MANE Select	NP_000739.1:p.Ala275=