Canonical Allele Identifier: CA497740298
Gene: CHRNB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7348461T>C (hg19)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000306071.7:c.15T>C MANE Select ENSP00000304290.2:p.Ala5=
ENST00000306071.6:c.15T>C ENSP00000304290.2:p.Ala5=
ENST00000572857.5:c.15T>C ENSP00000461402.1:p.Ala5=
ENST00000574054.1:n.35T>C
NM_000747.2:c.15T>C NP_000738.2:p.Ala5=
NM_000747.3:c.15T>C MANE Select NP_000738.2:p.Ala5=
Search 100 bp 5'
Search 100 bp 3'