Canonical Allele Identifier: CA2480925342

Gene: CHRNB2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.154571698_154571700delinsTCG , CM000663.2:g.154571698_154571700delinsTCG	GRCh38
NC_000001.10:g.154544174_154544176delinsTCG , CM000663.1:g.154544174_154544176delinsTCG	GRCh37
NC_000001.9:g.152810798_152810800delinsTCG	NCBI36
NG_008027.1:g.8918_8920delinsTCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368476.4:c.875_877delinsTCG MANE Select	ENSP00000357461.3:p.Leu292=
ENST00000636034.1:c.875_877delinsTCG	ENSP00000489703.1:p.Leu292=
ENST00000637900.1:c.881_883delinsTCG	ENSP00000490474.1:p.Leu294=
ENST00000368476.3:c.875_877delinsTCG	ENSP00000357461.3:p.Leu292=
NM_000748.2:c.875_877delinsTCG	NP_000739.1:p.Leu292=
XM_017000180.2:c.365_367delinsTCG	XP_016855669.1:p.Leu122=
XR_001736952.2:n.1127_1129delinsTCG
NM_000748.3:c.875_877delinsTCG MANE Select	NP_000739.1:p.Leu292=