Canonical Allele Identifier: CA2528334576

Gene: CHRNB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42732835_42732836insT , CM000670.2:g.42732835_42732836insT	GRCh38
NC_000008.10:g.42587978_42587979insT , CM000670.1:g.42587978_42587979insT	GRCh37
NC_000008.9:g.42707135_42707136insT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289957.3:c.1242+286_1242+287insT MANE Select	ENSP00000289957.2:n.1242+286_1242+287insT
ENST00000289957.2:c.1242+286_1242+287insT	ENSP00000289957.2:n.1242+286_1242+287insT
NM_000749.3:c.1242+286_1242+287insT	NP_000740.1:n.1242+286_1242+287insT
XM_011544390.1:c.855+286_855+287insT	XP_011542692.1:n.855+286_855+287insT
NM_000749.4:c.1242+286_1242+287insT	NP_000740.1:n.1242+286_1242+287insT
NM_001347717.1:c.1020+286_1020+287insT	NP_001334646.1:n.1020+286_1020+287insT
XM_011544390.2:c.855+286_855+287insT	XP_011542692.1:n.855+286_855+287insT
NM_000749.5:c.1242+286_1242+287insT MANE Select	NP_000740.1:n.1242+286_1242+287insT
NM_001347717.2:c.1020+286_1020+287insT	NP_001334646.1:n.1020+286_1020+287insT