Canonical Allele Identifier: CA1779564344

Gene: CHRNB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42732619_42732622delinsTTAC , CM000670.2:g.42732619_42732622delinsTTAC	GRCh38
NC_000008.10:g.42587762_42587765delinsTTAC , CM000670.1:g.42587762_42587765delinsTTAC	GRCh37
NC_000008.9:g.42706919_42706922delinsTTAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289957.3:c.1242+70_1242+73delinsTTAC MANE Select	ENSP00000289957.2:n.1242+70_1242+73delinsTTAC
ENST00000289957.2:c.1242+70_1242+73delinsTTAC	ENSP00000289957.2:n.1242+70_1242+73delinsTTAC
NM_000749.3:c.1242+70_1242+73delinsTTAC	NP_000740.1:n.1242+70_1242+73delinsTTAC
XM_011544390.1:c.855+70_855+73delinsTTAC	XP_011542692.1:n.855+70_855+73delinsTTAC
NM_000749.4:c.1242+70_1242+73delinsTTAC	NP_000740.1:n.1242+70_1242+73delinsTTAC
NM_001347717.1:c.1020+70_1020+73delinsTTAC	NP_001334646.1:n.1020+70_1020+73delinsTTAC
XM_011544390.2:c.855+70_855+73delinsTTAC	XP_011542692.1:n.855+70_855+73delinsTTAC
NM_000749.5:c.1242+70_1242+73delinsTTAC MANE Select	NP_000740.1:n.1242+70_1242+73delinsTTAC
NM_001347717.2:c.1020+70_1020+73delinsTTAC	NP_001334646.1:n.1020+70_1020+73delinsTTAC