Canonical Allele Identifier: CA497744727
Gene: CHRNB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7357833C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7454514C>A , CM000679.2:g.7454514C>A GRCh38
NC_000017.10:g.7357833C>A , CM000679.1:g.7357833C>A GRCh37
NC_000017.9:g.7298557C>A NCBI36
NG_008026.1:g.14428C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.1038C>A MANE Select ENSP00000304290.2:p.Val346=
ENST00000306071.6:c.1038C>A ENSP00000304290.2:p.Val346=
ENST00000536404.6:c.822C>A ENSP00000439209.2:p.Val274=
ENST00000570557.5:c.701C>A
ENST00000573209.1:n.1982C>A
ENST00000576360.1:c.675C>A ENSP00000459092.1:p.Val225=
NM_000747.2:c.1038C>A NP_000738.2:p.Val346=
NM_000747.3:c.1038C>A MANE Select NP_000738.2:p.Val346=
Search 100 bp 5'
Search 100 bp 3'