Canonical Allele Identifier: CA2635847051
Gene: CHRNB1 HGNC NCBI

Linked Data

gnomAD v4: 17-7455997-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7455997C>A , CM000679.2:g.7455997C>A GRCh38
NC_000017.10:g.7359316C>A , CM000679.1:g.7359316C>A GRCh37
NC_000017.9:g.7300040C>A NCBI36
NG_008026.1:g.15911C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.1365+56C>A MANE Select ENSP00000304290.2:n.1365+56C>A
ENST00000306071.6:c.1365+56C>A ENSP00000304290.2:n.1365+56C>A
ENST00000536404.6:c.1149+56C>A ENSP00000439209.2:n.1149+56C>A
ENST00000575379.1:c.-28+56C>A ENSP00000461751.1:n.-28+56C>A
ENST00000576360.1:c.1002+56C>A ENSP00000459092.1:n.1002+56C>A
NM_000747.2:c.1365+56C>A NP_000738.2:n.1365+56C>A
NM_000747.3:c.1365+56C>A MANE Select NP_000738.2:n.1365+56C>A
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