Canonical Allele Identifier: CA4734083
Gene: CHRNB3 HGNC NCBI

Linked Data

dbSNP Id: rs4953
ExAC: 8:42587659 G / A
gnomAD v2: 8-42587659-G-A
gnomAD v3: 8-42732516-G-A
gnomAD v4: 8-42732516-G-A
MyVariant Identifiers: chr8:g.42587659G>A (hg19) chr8:g.42732516G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42732516G>A , CM000670.2:g.42732516G>A GRCh38
NC_000008.10:g.42587659G>A , CM000670.1:g.42587659G>A GRCh37
NC_000008.9:g.42706816G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000289957.3:c.1209G>A MANE Select ENSP00000289957.2:p.Ser403=
ENST00000289957.2:c.1209G>A ENSP00000289957.2:p.Ser403=
NM_000749.3:c.1209G>A NP_000740.1:p.Ser403=
XM_011544390.1:c.822G>A XP_011542692.1:p.Ser274=
NM_000749.4:c.1209G>A NP_000740.1:p.Ser403=
NM_001347717.1:c.987G>A NP_001334646.1:p.Ser329=
XM_011544390.2:c.822G>A XP_011542692.1:p.Ser274=
NM_000749.5:c.1209G>A MANE Select NP_000740.1:p.Ser403=
NM_001347717.2:c.987G>A NP_001334646.1:p.Ser329=
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