Canonical Allele Identifier: CA774956919
Gene: CHRNB1 HGNC NCBI

Linked Data

dbSNP Id: rs1293715818
gnomAD v4: 17-7454546-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7454546C>A , CM000679.2:g.7454546C>A GRCh38
NC_000017.10:g.7357865C>A , CM000679.1:g.7357865C>A GRCh37
NC_000017.9:g.7298589C>A NCBI36
NG_008026.1:g.14460C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.1044+26C>A MANE Select ENSP00000304290.2:n.1044+26C>A
ENST00000306071.6:c.1044+26C>A ENSP00000304290.2:n.1044+26C>A
ENST00000536404.6:c.828+26C>A ENSP00000439209.2:n.828+26C>A
ENST00000570557.5:c.707+26C>A
ENST00000573209.1:n.1988+26C>A
ENST00000576360.1:c.681+26C>A ENSP00000459092.1:n.681+26C>A
NM_000747.2:c.1044+26C>A NP_000738.2:n.1044+26C>A
NM_000747.3:c.1044+26C>A MANE Select NP_000738.2:n.1044+26C>A