Canonical Allele Identifier: CA2480925221

Gene: CHRNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571335T= , CM000663.2:g.154571335T=	GRCh38
NC_000001.10:g.154543811T= , CM000663.1:g.154543811T=	GRCh37
NC_000001.9:g.152810435T=	NCBI36
NG_008027.1:g.8555T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.512T= MANE Select	ENSP00000357461.3:p.Met171=
ENST00000636034.1:c.512T=	ENSP00000489703.1:p.Met171=
ENST00000637900.1:c.518T=	ENSP00000490474.1:p.Met173=
ENST00000368476.3:c.512T=	ENSP00000357461.3:p.Met171=
NM_000748.2:c.512T=	NP_000739.1:p.Met171=
XM_017000180.2:c.2T=	XP_016855669.1:p.Met1=
XR_001736952.2:n.764T=
NM_000748.3:c.512T= MANE Select	NP_000739.1:p.Met171=