Canonical Allele Identifier: CA342630661
Gene: CHRNB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.154544005T>A (hg19) chr1:g.154571529T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571529T>A , CM000663.2:g.154571529T>A GRCh38
NC_000001.10:g.154544005T>A , CM000663.1:g.154544005T>A GRCh37
NC_000001.9:g.152810629T>A NCBI36
NG_008027.1:g.8749T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.706T>A MANE Select ENSP00000357461.3:p.Phe236Ile
ENST00000636034.1:c.706T>A ENSP00000489703.1:p.Phe236Ile
ENST00000637900.1:c.712T>A ENSP00000490474.1:p.Phe238Ile
ENST00000368476.3:c.706T>A ENSP00000357461.3:p.Phe236Ile
NM_000748.2:c.706T>A NP_000739.1:p.Phe236Ile
XM_017000180.2:c.196T>A XP_016855669.1:p.Phe66Ile
XR_001736952.2:n.958T>A
NM_000748.3:c.706T>A MANE Select NP_000739.1:p.Phe236Ile
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