Canonical Allele Identifier: CA2733119278
Gene: CHRNB1 HGNC NCBI

Linked Data

dbSNP Id: rs2150842239
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7454062A>C , CM000679.2:g.7454062A>C GRCh38
NC_000017.10:g.7357381A>C , CM000679.1:g.7357381A>C GRCh37
NC_000017.9:g.7298105A>C NCBI36
NG_008026.1:g.13976A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.821-235A>C MANE Select ENSP00000304290.2:n.821-235A>C
ENST00000306071.6:c.821-235A>C ENSP00000304290.2:n.821-235A>C
ENST00000536404.6:c.605-235A>C ENSP00000439209.2:n.605-235A>C
ENST00000570557.5:c.484-235A>C
ENST00000573209.1:n.1765-235A>C
ENST00000576360.1:c.605-382A>C ENSP00000459092.1:n.605-382A>C
NM_000747.2:c.821-235A>C NP_000738.2:n.821-235A>C
NM_000747.3:c.821-235A>C MANE Select NP_000738.2:n.821-235A>C
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