Canonical Allele Identifier: CA2480925368

Gene: CHRNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571752_154571753delinsTC , CM000663.2:g.154571752_154571753delinsTC	GRCh38
NC_000001.10:g.154544228_154544229delinsTC , CM000663.1:g.154544228_154544229delinsTC	GRCh37
NC_000001.9:g.152810852_152810853delinsTC	NCBI36
NG_008027.1:g.8972_8973delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.929_930delinsTC MANE Select	ENSP00000357461.3:p.Phe310=
ENST00000636034.1:c.929_930delinsTC	ENSP00000489703.1:p.Phe310=
ENST00000637900.1:c.935_936delinsTC	ENSP00000490474.1:p.Phe312=
ENST00000368476.3:c.929_930delinsTC	ENSP00000357461.3:p.Phe310=
NM_000748.2:c.929_930delinsTC	NP_000739.1:p.Phe310=
XM_017000180.2:c.419_420delinsTC	XP_016855669.1:p.Phe140=
XR_001736952.2:n.1181_1182delinsTC
NM_000748.3:c.929_930delinsTC MANE Select	NP_000739.1:p.Phe310=