Canonical Allele Identifier: CA4734094
Gene: CHRNB3 HGNC NCBI

Linked Data

dbSNP Id: rs113912284
ExAC: 8:42587725 G / A
gnomAD v2: 8-42587725-G-A
gnomAD v3: 8-42732582-G-A
gnomAD v4: 8-42732582-G-A
MyVariant Identifiers: chr8:g.42587725G>A (hg19) chr8:g.42732582G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42732582G>A , CM000670.2:g.42732582G>A GRCh38
NC_000008.10:g.42587725G>A , CM000670.1:g.42587725G>A GRCh37
NC_000008.9:g.42706882G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000289957.3:c.1242+33G>A MANE Select ENSP00000289957.2:n.1242+33G>A
ENST00000289957.2:c.1242+33G>A ENSP00000289957.2:n.1242+33G>A
NM_000749.3:c.1242+33G>A NP_000740.1:n.1242+33G>A
XM_011544390.1:c.855+33G>A XP_011542692.1:n.855+33G>A
NM_000749.4:c.1242+33G>A NP_000740.1:n.1242+33G>A
NM_001347717.1:c.1020+33G>A NP_001334646.1:n.1020+33G>A
XM_011544390.2:c.855+33G>A XP_011542692.1:n.855+33G>A
NM_000749.5:c.1242+33G>A MANE Select NP_000740.1:n.1242+33G>A
NM_001347717.2:c.1020+33G>A NP_001334646.1:n.1020+33G>A
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