Canonical Allele Identifier: CA2480925226

Gene: CHRNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571348G= , CM000663.2:g.154571348G=	GRCh38
NC_000001.10:g.154543824G= , CM000663.1:g.154543824G=	GRCh37
NC_000001.9:g.152810448G=	NCBI36
NG_008027.1:g.8568G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.525G= MANE Select	ENSP00000357461.3:p.Ser175=
ENST00000636034.1:c.525G=	ENSP00000489703.1:p.Ser175=
ENST00000637900.1:c.531G=	ENSP00000490474.1:p.Ser177=
ENST00000368476.3:c.525G=	ENSP00000357461.3:p.Ser175=
NM_000748.2:c.525G=	NP_000739.1:p.Ser175=
XM_017000180.2:c.15G=	XP_016855669.1:p.Ser5=
XR_001736952.2:n.777G=
NM_000748.3:c.525G= MANE Select	NP_000739.1:p.Ser175=