Canonical Allele Identifier: CA1779564472

Gene: CHRNB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42732833_42732834delinsTC , CM000670.2:g.42732833_42732834delinsTC	GRCh38
NC_000008.10:g.42587976_42587977delinsTC , CM000670.1:g.42587976_42587977delinsTC	GRCh37
NC_000008.9:g.42707133_42707134delinsTC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289957.3:c.1242+284_1242+285delinsTC MANE Select	ENSP00000289957.2:n.1242+284_1242+285delinsTC
ENST00000289957.2:c.1242+284_1242+285delinsTC	ENSP00000289957.2:n.1242+284_1242+285delinsTC
NM_000749.3:c.1242+284_1242+285delinsTC	NP_000740.1:n.1242+284_1242+285delinsTC
XM_011544390.1:c.855+284_855+285delinsTC	XP_011542692.1:n.855+284_855+285delinsTC
NM_000749.4:c.1242+284_1242+285delinsTC	NP_000740.1:n.1242+284_1242+285delinsTC
NM_001347717.1:c.1020+284_1020+285delinsTC	NP_001334646.1:n.1020+284_1020+285delinsTC
XM_011544390.2:c.855+284_855+285delinsTC	XP_011542692.1:n.855+284_855+285delinsTC
NM_000749.5:c.1242+284_1242+285delinsTC MANE Select	NP_000740.1:n.1242+284_1242+285delinsTC
NM_001347717.2:c.1020+284_1020+285delinsTC	NP_001334646.1:n.1020+284_1020+285delinsTC