Canonical Allele Identifier: CA497740293
Gene: CHRNB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7348461T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7445142T>A , CM000679.2:g.7445142T>A GRCh38
NC_000017.10:g.7348461T>A , CM000679.1:g.7348461T>A GRCh37
NC_000017.9:g.7289185T>A NCBI36
NG_008026.1:g.5056T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000306071.7:c.15T>A MANE Select ENSP00000304290.2:p.Ala5=
ENST00000306071.6:c.15T>A ENSP00000304290.2:p.Ala5=
ENST00000572857.5:c.15T>A ENSP00000461402.1:p.Ala5=
ENST00000574054.1:n.35T>A
NM_000747.2:c.15T>A NP_000738.2:p.Ala5=
NM_000747.3:c.15T>A MANE Select NP_000738.2:p.Ala5=