Canonical Allele Identifier: CA2480925181

Gene: CHRNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571199A= , CM000663.2:g.154571199A=	GRCh38
NC_000001.10:g.154543675A= , CM000663.1:g.154543675A=	GRCh37
NC_000001.9:g.152810299A=	NCBI36
NG_008027.1:g.8419A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.376A= MANE Select	ENSP00000357461.3:p.Met126=
ENST00000636034.1:c.376A=	ENSP00000489703.1:p.Met126=
ENST00000637900.1:c.382A=	ENSP00000490474.1:p.Met128=
ENST00000368476.3:c.376A=	ENSP00000357461.3:p.Met126=
NM_000748.2:c.376A=	NP_000739.1:p.Met126=
XM_017000180.2:c.-9-126A=	XP_016855669.1:n.-9-126A=
XR_001736952.2:n.628A=
NM_000748.3:c.376A= MANE Select	NP_000739.1:p.Met126=