Canonical Allele Identifier: CA2245821935
Gene: CHRNB1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7454572G= , CM000679.2:g.7454572G= GRCh38
NC_000017.10:g.7357891G= , CM000679.1:g.7357891G= GRCh37
NC_000017.9:g.7298615G= NCBI36
NG_008026.1:g.14486G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.1044+52G= MANE Select ENSP00000304290.2:n.1044+52G=
ENST00000306071.6:c.1044+52G= ENSP00000304290.2:n.1044+52G=
ENST00000536404.6:c.828+52G= ENSP00000439209.2:n.828+52G=
ENST00000570557.5:c.707+52G=
ENST00000573209.1:n.1988+52G=
ENST00000576360.1:c.681+52G= ENSP00000459092.1:n.681+52G=
NM_000747.2:c.1044+52G= NP_000738.2:n.1044+52G=
NM_000747.3:c.1044+52G= MANE Select NP_000738.2:n.1044+52G=
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