Canonical Allele Identifier: CA2245821922
Gene: CHRNB1 HGNC NCBI

Linked Data

dbSNP Id: rs7210231

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7454545C>G , CM000679.2:g.7454545C>G GRCh38
NC_000017.10:g.7357864C>G , CM000679.1:g.7357864C>G GRCh37
NC_000017.9:g.7298588C>G NCBI36
NG_008026.1:g.14459C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.1044+25C>G MANE Select ENSP00000304290.2:n.1044+25C>G
ENST00000306071.6:c.1044+25C>G ENSP00000304290.2:n.1044+25C>G
ENST00000536404.6:c.828+25C>G ENSP00000439209.2:n.828+25C>G
ENST00000570557.5:c.707+25C>G
ENST00000573209.1:n.1988+25C>G
ENST00000576360.1:c.681+25C>G ENSP00000459092.1:n.681+25C>G
NM_000747.2:c.1044+25C>G NP_000738.2:n.1044+25C>G
NM_000747.3:c.1044+25C>G MANE Select NP_000738.2:n.1044+25C>G