Canonical Allele Identifier: CA2245821724
Gene: CHRNB1 HGNC NCBI

Linked Data

dbSNP Id: rs1908983836
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7454078A>G , CM000679.2:g.7454078A>G GRCh38
NC_000017.10:g.7357397A>G , CM000679.1:g.7357397A>G GRCh37
NC_000017.9:g.7298121A>G NCBI36
NG_008026.1:g.13992A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.821-219A>G MANE Select ENSP00000304290.2:n.821-219A>G
ENST00000306071.6:c.821-219A>G ENSP00000304290.2:n.821-219A>G
ENST00000536404.6:c.605-219A>G ENSP00000439209.2:n.605-219A>G
ENST00000570557.5:c.484-219A>G
ENST00000573209.1:n.1765-219A>G
ENST00000576360.1:c.605-366A>G ENSP00000459092.1:n.605-366A>G
NM_000747.2:c.821-219A>G NP_000738.2:n.821-219A>G
NM_000747.3:c.821-219A>G MANE Select NP_000738.2:n.821-219A>G
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