Canonical Allele Identifier: CA1779564238

Gene: CHRNB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42732520_42732522delinsCAT , CM000670.2:g.42732520_42732522delinsCAT	GRCh38
NC_000008.10:g.42587663_42587665delinsCAT , CM000670.1:g.42587663_42587665delinsCAT	GRCh37
NC_000008.9:g.42706820_42706822delinsCAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289957.3:c.1213_1215delinsCAT MANE Select	ENSP00000289957.2:p.His405=
ENST00000289957.2:c.1213_1215delinsCAT	ENSP00000289957.2:p.His405=
NM_000749.3:c.1213_1215delinsCAT	NP_000740.1:p.His405=
XM_011544390.1:c.826_828delinsCAT	XP_011542692.1:p.His276=
NM_000749.4:c.1213_1215delinsCAT	NP_000740.1:p.His405=
NM_001347717.1:c.991_993delinsCAT	NP_001334646.1:p.His331=
XM_011544390.2:c.826_828delinsCAT	XP_011542692.1:p.His276=
NM_000749.5:c.1213_1215delinsCAT MANE Select	NP_000740.1:p.His405=
NM_001347717.2:c.991_993delinsCAT	NP_001334646.1:p.His331=