Canonical Allele Identifier: CA397786160
Gene: CHRNB1 HGNC NCBI

Linked Data

dbSNP Id: rs1908541089
MyVariant Identifiers: chr17:g.7348457G>A (hg19) chr17:g.7445138G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7445138G>A , CM000679.2:g.7445138G>A GRCh38
NC_000017.10:g.7348457G>A , CM000679.1:g.7348457G>A GRCh37
NC_000017.9:g.7289181G>A NCBI36
NG_008026.1:g.5052G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000306071.7:c.11G>A MANE Select ENSP00000304290.2:p.Gly4Glu
ENST00000306071.6:c.11G>A ENSP00000304290.2:p.Gly4Glu
ENST00000572857.5:c.11G>A ENSP00000461402.1:p.Gly4Glu
ENST00000574054.1:n.31G>A
NM_000747.2:c.11G>A NP_000738.2:p.Gly4Glu
NM_000747.3:c.11G>A MANE Select NP_000738.2:p.Gly4Glu
Search 100 bp 5'
Search 100 bp 3'