Canonical Allele Identifier: CA497744709
Gene: CHRNB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7357803A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7454484A>T , CM000679.2:g.7454484A>T GRCh38
NC_000017.10:g.7357803A>T , CM000679.1:g.7357803A>T GRCh37
NC_000017.9:g.7298527A>T NCBI36
NG_008026.1:g.14398A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.1008A>T MANE Select ENSP00000304290.2:p.Ser336=
ENST00000306071.6:c.1008A>T ENSP00000304290.2:p.Ser336=
ENST00000536404.6:c.792A>T ENSP00000439209.2:p.Ser264=
ENST00000570557.5:c.671A>T
ENST00000573209.1:n.1952A>T
ENST00000576360.1:c.645A>T ENSP00000459092.1:p.Ser215=
NM_000747.2:c.1008A>T NP_000738.2:p.Ser336=
NM_000747.3:c.1008A>T MANE Select NP_000738.2:p.Ser336=