Canonical Allele Identifier: CA397797477
Gene: CHRNB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7454365A>G , CM000679.2:g.7454365A>G GRCh38
NC_000017.10:g.7357684A>G , CM000679.1:g.7357684A>G GRCh37
NC_000017.9:g.7298408A>G NCBI36
NG_008026.1:g.14279A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.889A>G MANE Select ENSP00000304290.2:p.Lys297Glu
ENST00000306071.6:c.889A>G ENSP00000304290.2:p.Lys297Glu
ENST00000536404.6:c.673A>G ENSP00000439209.2:p.Lys225Glu
ENST00000570557.5:c.552A>G
ENST00000573209.1:n.1833A>G
ENST00000576360.1:c.605-79A>G ENSP00000459092.1:n.605-79A>G
NM_000747.2:c.889A>G NP_000738.2:p.Lys297Glu
NM_000747.3:c.889A>G MANE Select NP_000738.2:p.Lys297Glu