Canonical Allele Identifier: CA421231389
Gene: CHRNB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.154544241C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571765C>A , CM000663.2:g.154571765C>A GRCh38
NC_000001.10:g.154544241C>A , CM000663.1:g.154544241C>A GRCh37
NC_000001.9:g.152810865C>A NCBI36
NG_008027.1:g.8985C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.942C>A MANE Select ENSP00000357461.3:p.Thr314=
ENST00000636034.1:c.942C>A ENSP00000489703.1:p.Thr314=
ENST00000637900.1:c.948C>A ENSP00000490474.1:p.Thr316=
ENST00000368476.3:c.942C>A ENSP00000357461.3:p.Thr314=
NM_000748.2:c.942C>A NP_000739.1:p.Thr314=
XM_017000180.2:c.432C>A XP_016855669.1:p.Thr144=
XR_001736952.2:n.1194C>A
NM_000748.3:c.942C>A MANE Select NP_000739.1:p.Thr314=
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