Canonical Allele Identifier: CA1779564254

Gene: CHRNB3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42732529_42732532delinsAAAG , CM000670.2:g.42732529_42732532delinsAAAG	GRCh38
NC_000008.10:g.42587672_42587675delinsAAAG , CM000670.1:g.42587672_42587675delinsAAAG	GRCh37
NC_000008.9:g.42706829_42706832delinsAAAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289957.3:c.1222_1225delinsAAAG MANE Select	ENSP00000289957.2:p.Lys408=
ENST00000289957.2:c.1222_1225delinsAAAG	ENSP00000289957.2:p.Lys408=
NM_000749.3:c.1222_1225delinsAAAG	NP_000740.1:p.Lys408=
XM_011544390.1:c.835_838delinsAAAG	XP_011542692.1:p.Lys279=
NM_000749.4:c.1222_1225delinsAAAG	NP_000740.1:p.Lys408=
NM_001347717.1:c.1000_1003delinsAAAG	NP_001334646.1:p.Lys334=
XM_011544390.2:c.835_838delinsAAAG	XP_011542692.1:p.Lys279=
NM_000749.5:c.1222_1225delinsAAAG MANE Select	NP_000740.1:p.Lys408=
NM_001347717.2:c.1000_1003delinsAAAG	NP_001334646.1:p.Lys334=