Canonical Allele Identifier: CA397798660
Gene: CHRNB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7454479C>A , CM000679.2:g.7454479C>A GRCh38
NC_000017.10:g.7357798C>A , CM000679.1:g.7357798C>A GRCh37
NC_000017.9:g.7298522C>A NCBI36
NG_008026.1:g.14393C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.1003C>A MANE Select ENSP00000304290.2:p.Arg335Ser
ENST00000306071.6:c.1003C>A ENSP00000304290.2:p.Arg335Ser
ENST00000536404.6:c.787C>A ENSP00000439209.2:p.Arg263Ser
ENST00000570557.5:c.666C>A
ENST00000573209.1:n.1947C>A
ENST00000576360.1:c.640C>A ENSP00000459092.1:p.Arg214Ser
NM_000747.2:c.1003C>A NP_000738.2:p.Arg335Ser
NM_000747.3:c.1003C>A MANE Select NP_000738.2:p.Arg335Ser