Canonical Allele Identifier: CA342630269
Gene: CHRNB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.154543841C>A (hg19) chr1:g.154571365C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571365C>A , CM000663.2:g.154571365C>A GRCh38
NC_000001.10:g.154543841C>A , CM000663.1:g.154543841C>A GRCh37
NC_000001.9:g.152810465C>A NCBI36
NG_008027.1:g.8585C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.542C>A MANE Select ENSP00000357461.3:p.Thr181Lys
ENST00000636034.1:c.542C>A ENSP00000489703.1:p.Thr181Lys
ENST00000637900.1:c.548C>A ENSP00000490474.1:p.Thr183Lys
ENST00000368476.3:c.542C>A ENSP00000357461.3:p.Thr181Lys
NM_000748.2:c.542C>A NP_000739.1:p.Thr181Lys
XM_017000180.2:c.32C>A XP_016855669.1:p.Thr11Lys
XR_001736952.2:n.794C>A
NM_000748.3:c.542C>A MANE Select NP_000739.1:p.Thr181Lys
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