Canonical Allele Identifier: CA397802017
Gene: CHRNB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7359114T>A (hg19) chr17:g.7455795T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7455795T>A , CM000679.2:g.7455795T>A GRCh38
NC_000017.10:g.7359114T>A , CM000679.1:g.7359114T>A GRCh37
NC_000017.9:g.7299838T>A NCBI36
NG_008026.1:g.15709T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.1219T>A MANE Select ENSP00000304290.2:p.Phe407Ile
ENST00000306071.6:c.1219T>A ENSP00000304290.2:p.Phe407Ile
ENST00000536404.6:c.1003T>A ENSP00000439209.2:p.Phe335Ile
ENST00000570557.5:c.882T>A
ENST00000575379.1:c.-174T>A ENSP00000461751.1:n.-174T>A
ENST00000576360.1:c.856T>A ENSP00000459092.1:p.Phe286Ile
NM_000747.2:c.1219T>A NP_000738.2:p.Phe407Ile
NM_000747.3:c.1219T>A MANE Select NP_000738.2:p.Phe407Ile
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