Canonical Allele Identifier: CA1113234877
Gene: CHRNB3 HGNC NCBI

Linked Data

dbSNP Id: rs1816454638
gnomAD v3: 8-42732899-A-G
gnomAD v4: 8-42732899-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42732899A>G , CM000670.2:g.42732899A>G GRCh38
NC_000008.10:g.42588042A>G , CM000670.1:g.42588042A>G GRCh37
NC_000008.9:g.42707199A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000289957.3:c.1242+350A>G MANE Select ENSP00000289957.2:n.1242+350A>G
ENST00000289957.2:c.1242+350A>G ENSP00000289957.2:n.1242+350A>G
NM_000749.3:c.1242+350A>G NP_000740.1:n.1242+350A>G
XM_011544390.1:c.855+350A>G XP_011542692.1:n.855+350A>G
NM_000749.4:c.1242+350A>G NP_000740.1:n.1242+350A>G
NM_001347717.1:c.1020+350A>G NP_001334646.1:n.1020+350A>G
XM_011544390.2:c.855+350A>G XP_011542692.1:n.855+350A>G
NM_000749.5:c.1242+350A>G MANE Select NP_000740.1:n.1242+350A>G
NM_001347717.2:c.1020+350A>G NP_001334646.1:n.1020+350A>G
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