Canonical Allele Identifier: CA342630160
Gene: CHRNB2 HGNC NCBI

Linked Data

gnomAD v4: 1-154571319-C-G
MyVariant Identifiers: chr1:g.154543795C>G (hg19) chr1:g.154571319C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571319C>G , CM000663.2:g.154571319C>G GRCh38
NC_000001.10:g.154543795C>G , CM000663.1:g.154543795C>G GRCh37
NC_000001.9:g.152810419C>G NCBI36
NG_008027.1:g.8539C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.496C>G MANE Select ENSP00000357461.3:p.Gln166Glu
ENST00000636034.1:c.496C>G ENSP00000489703.1:p.Gln166Glu
ENST00000637900.1:c.502C>G ENSP00000490474.1:p.Gln168Glu
ENST00000368476.3:c.496C>G ENSP00000357461.3:p.Gln166Glu
NM_000748.2:c.496C>G NP_000739.1:p.Gln166Glu
XM_017000180.2:c.-9-6C>G XP_016855669.1:n.-9-6C>G
XR_001736952.2:n.748C>G
NM_000748.3:c.496C>G MANE Select NP_000739.1:p.Gln166Glu
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