Canonical Allele Identifier: CA2245822646
Gene: CHRNB1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7455992A= , CM000679.2:g.7455992A= GRCh38
NC_000017.10:g.7359311A= , CM000679.1:g.7359311A= GRCh37
NC_000017.9:g.7300035A= NCBI36
NG_008026.1:g.15906A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.1365+51A= MANE Select ENSP00000304290.2:n.1365+51A=
ENST00000306071.6:c.1365+51A= ENSP00000304290.2:n.1365+51A=
ENST00000536404.6:c.1149+51A= ENSP00000439209.2:n.1149+51A=
ENST00000575379.1:c.-28+51A= ENSP00000461751.1:n.-28+51A=
ENST00000576360.1:c.1002+51A= ENSP00000459092.1:n.1002+51A=
NM_000747.2:c.1365+51A= NP_000738.2:n.1365+51A=
NM_000747.3:c.1365+51A= MANE Select NP_000738.2:n.1365+51A=
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