Canonical Allele Identifier: CA397797911
Gene: CHRNB1 HGNC NCBI

Linked Data

dbSNP Id: rs1326483709
gnomAD v2: 17-7357724-A-G
gnomAD v4: 17-7454405-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7454405A>G , CM000679.2:g.7454405A>G GRCh38
NC_000017.10:g.7357724A>G , CM000679.1:g.7357724A>G GRCh37
NC_000017.9:g.7298448A>G NCBI36
NG_008026.1:g.14319A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.929A>G MANE Select ENSP00000304290.2:p.Lys310Arg
ENST00000306071.6:c.929A>G ENSP00000304290.2:p.Lys310Arg
ENST00000536404.6:c.713A>G ENSP00000439209.2:p.Lys238Arg
ENST00000570557.5:c.592A>G
ENST00000573209.1:n.1873A>G
ENST00000576360.1:c.605-39A>G ENSP00000459092.1:n.605-39A>G
NM_000747.2:c.929A>G NP_000738.2:p.Lys310Arg
NM_000747.3:c.929A>G MANE Select NP_000738.2:p.Lys310Arg