Canonical Allele Identifier: CA342631153
Gene: CHRNB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.154544240C>A (hg19) chr1:g.154571764C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571764C>A , CM000663.2:g.154571764C>A GRCh38
NC_000001.10:g.154544240C>A , CM000663.1:g.154544240C>A GRCh37
NC_000001.9:g.152810864C>A NCBI36
NG_008027.1:g.8984C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.941C>A MANE Select ENSP00000357461.3:p.Thr314Asn
ENST00000636034.1:c.941C>A ENSP00000489703.1:p.Thr314Asn
ENST00000637900.1:c.947C>A ENSP00000490474.1:p.Thr316Asn
ENST00000368476.3:c.941C>A ENSP00000357461.3:p.Thr314Asn
NM_000748.2:c.941C>A NP_000739.1:p.Thr314Asn
XM_017000180.2:c.431C>A XP_016855669.1:p.Thr144Asn
XR_001736952.2:n.1193C>A
NM_000748.3:c.941C>A MANE Select NP_000739.1:p.Thr314Asn
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