Canonical Allele Identifier: CA397798787
Gene: CHRNB1 HGNC NCBI

Linked Data

gnomAD v4: 17-7454492-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7454492C>A , CM000679.2:g.7454492C>A GRCh38
NC_000017.10:g.7357811C>A , CM000679.1:g.7357811C>A GRCh37
NC_000017.9:g.7298535C>A NCBI36
NG_008026.1:g.14406C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.1016C>A MANE Select ENSP00000304290.2:p.Thr339Asn
ENST00000306071.6:c.1016C>A ENSP00000304290.2:p.Thr339Asn
ENST00000536404.6:c.800C>A ENSP00000439209.2:p.Thr267Asn
ENST00000570557.5:c.679C>A
ENST00000573209.1:n.1960C>A
ENST00000576360.1:c.653C>A ENSP00000459092.1:p.Thr218Asn
NM_000747.2:c.1016C>A NP_000738.2:p.Thr339Asn
NM_000747.3:c.1016C>A MANE Select NP_000738.2:p.Thr339Asn