Canonical Allele Identifier: CA1779564320

Gene: CHRNB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42732583_42732584delinsTA , CM000670.2:g.42732583_42732584delinsTA	GRCh38
NC_000008.10:g.42587726_42587727delinsTA , CM000670.1:g.42587726_42587727delinsTA	GRCh37
NC_000008.9:g.42706883_42706884delinsTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289957.3:c.1242+34_1242+35delinsTA MANE Select	ENSP00000289957.2:n.1242+34_1242+35delinsTA
ENST00000289957.2:c.1242+34_1242+35delinsTA	ENSP00000289957.2:n.1242+34_1242+35delinsTA
NM_000749.3:c.1242+34_1242+35delinsTA	NP_000740.1:n.1242+34_1242+35delinsTA
XM_011544390.1:c.855+34_855+35delinsTA	XP_011542692.1:n.855+34_855+35delinsTA
NM_000749.4:c.1242+34_1242+35delinsTA	NP_000740.1:n.1242+34_1242+35delinsTA
NM_001347717.1:c.1020+34_1020+35delinsTA	NP_001334646.1:n.1020+34_1020+35delinsTA
XM_011544390.2:c.855+34_855+35delinsTA	XP_011542692.1:n.855+34_855+35delinsTA
NM_000749.5:c.1242+34_1242+35delinsTA MANE Select	NP_000740.1:n.1242+34_1242+35delinsTA
NM_001347717.2:c.1020+34_1020+35delinsTA	NP_001334646.1:n.1020+34_1020+35delinsTA