Canonical Allele Identifier: CA2245821719
Gene: CHRNB1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7454056G= , CM000679.2:g.7454056G= GRCh38
NC_000017.10:g.7357375G= , CM000679.1:g.7357375G= GRCh37
NC_000017.9:g.7298099G= NCBI36
NG_008026.1:g.13970G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.821-241G= MANE Select ENSP00000304290.2:n.821-241G=
ENST00000306071.6:c.821-241G= ENSP00000304290.2:n.821-241G=
ENST00000536404.6:c.605-241G= ENSP00000439209.2:n.605-241G=
ENST00000570557.5:c.484-241G=
ENST00000573209.1:n.1765-241G=
ENST00000576360.1:c.605-388G= ENSP00000459092.1:n.605-388G=
NM_000747.2:c.821-241G= NP_000738.2:n.821-241G=
NM_000747.3:c.821-241G= MANE Select NP_000738.2:n.821-241G=
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