Canonical Allele Identifier: CA497740278
Gene: CHRNB1 HGNC NCBI

Linked Data

dbSNP Id: rs1908541265
gnomAD v4: 17-7445139-G-A
MyVariant Identifiers: chr17:g.7348458G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7445139G>A , CM000679.2:g.7445139G>A GRCh38
NC_000017.10:g.7348458G>A , CM000679.1:g.7348458G>A GRCh37
NC_000017.9:g.7289182G>A NCBI36
NG_008026.1:g.5053G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000306071.7:c.12G>A MANE Select ENSP00000304290.2:p.Gly4=
ENST00000306071.6:c.12G>A ENSP00000304290.2:p.Gly4=
ENST00000572857.5:c.12G>A ENSP00000461402.1:p.Gly4=
ENST00000574054.1:n.32G>A
NM_000747.2:c.12G>A NP_000738.2:p.Gly4=
NM_000747.3:c.12G>A MANE Select NP_000738.2:p.Gly4=