Canonical Allele Identifier: CA2245821715
Gene: CHRNB1 HGNC NCBI

Linked Data

dbSNP Id: rs1908983038
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7454047C>A , CM000679.2:g.7454047C>A GRCh38
NC_000017.10:g.7357366C>A , CM000679.1:g.7357366C>A GRCh37
NC_000017.9:g.7298090C>A NCBI36
NG_008026.1:g.13961C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.821-250C>A MANE Select ENSP00000304290.2:n.821-250C>A
ENST00000306071.6:c.821-250C>A ENSP00000304290.2:n.821-250C>A
ENST00000536404.6:c.605-250C>A ENSP00000439209.2:n.605-250C>A
ENST00000570557.5:c.484-250C>A
ENST00000573209.1:n.1765-250C>A
ENST00000576360.1:c.605-397C>A ENSP00000459092.1:n.605-397C>A
NM_000747.2:c.821-250C>A NP_000738.2:n.821-250C>A
NM_000747.3:c.821-250C>A MANE Select NP_000738.2:n.821-250C>A
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