Canonical Allele Identifier: CA397799089
Gene: CHRNB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7454522T>G , CM000679.2:g.7454522T>G GRCh38
NC_000017.10:g.7357841T>G , CM000679.1:g.7357841T>G GRCh37
NC_000017.9:g.7298565T>G NCBI36
NG_008026.1:g.14436T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.1044+2T>G MANE Select ENSP00000304290.2:n.1044+2T>G
ENST00000306071.6:c.1044+2T>G ENSP00000304290.2:n.1044+2T>G
ENST00000536404.6:c.828+2T>G ENSP00000439209.2:n.828+2T>G
ENST00000570557.5:c.707+2T>G
ENST00000573209.1:n.1988+2T>G
ENST00000576360.1:c.681+2T>G ENSP00000459092.1:n.681+2T>G
NM_000747.2:c.1044+2T>G NP_000738.2:n.1044+2T>G
NM_000747.3:c.1044+2T>G MANE Select NP_000738.2:n.1044+2T>G