Canonical Allele Identifier: CA2245821914

Gene: CHRNB1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7454531_7454534delinsTCTC , CM000679.2:g.7454531_7454534delinsTCTC	GRCh38
NC_000017.10:g.7357850_7357853delinsTCTC , CM000679.1:g.7357850_7357853delinsTCTC	GRCh37
NC_000017.9:g.7298574_7298577delinsTCTC	NCBI36
NG_008026.1:g.14445_14448delinsTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306071.7:c.1044+11_1044+14delinsTCTC MANE Select	ENSP00000304290.2:n.1044+11_1044+14delinsTCTC
ENST00000306071.6:c.1044+11_1044+14delinsTCTC	ENSP00000304290.2:n.1044+11_1044+14delinsTCTC
ENST00000536404.6:c.828+11_828+14delinsTCTC	ENSP00000439209.2:n.828+11_828+14delinsTCTC
ENST00000570557.5:c.707+11_707+14delinsTCTC
ENST00000573209.1:n.1988+11_1988+14delinsTCTC
ENST00000576360.1:c.681+11_681+14delinsTCTC	ENSP00000459092.1:n.681+11_681+14delinsTCTC
NM_000747.2:c.1044+11_1044+14delinsTCTC	NP_000738.2:n.1044+11_1044+14delinsTCTC
NM_000747.3:c.1044+11_1044+14delinsTCTC MANE Select	NP_000738.2:n.1044+11_1044+14delinsTCTC