Canonical Allele Identifier: CA1779564416

Gene: CHRNB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42732718T= , CM000670.2:g.42732718T=	GRCh38
NC_000008.10:g.42587861T= , CM000670.1:g.42587861T=	GRCh37
NC_000008.9:g.42707018T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289957.3:c.1242+169T= MANE Select	ENSP00000289957.2:n.1242+169T=
ENST00000289957.2:c.1242+169T=	ENSP00000289957.2:n.1242+169T=
NM_000749.3:c.1242+169T=	NP_000740.1:n.1242+169T=
XM_011544390.1:c.855+169T=	XP_011542692.1:n.855+169T=
NM_000749.4:c.1242+169T=	NP_000740.1:n.1242+169T=
NM_001347717.1:c.1020+169T=	NP_001334646.1:n.1020+169T=
XM_011544390.2:c.855+169T=	XP_011542692.1:n.855+169T=
NM_000749.5:c.1242+169T= MANE Select	NP_000740.1:n.1242+169T=
NM_001347717.2:c.1020+169T=	NP_001334646.1:n.1020+169T=