Canonical Allele Identifier: CA1147949792
Gene: CHRNB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154576057T= , CM000663.2:g.154576057T= GRCh38
NC_000001.10:g.154548533T= , CM000663.1:g.154548533T= GRCh37
NC_000001.9:g.152815157T= NCBI36
NG_008027.1:g.13277T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.*125T= MANE Select ENSP00000357461.3:n.*125T=
ENST00000636034.1:c.1505+129T= ENSP00000489703.1:n.1505+129T=
ENST00000637900.1:c.*125T= ENSP00000490474.1:n.*125T=
ENST00000368476.3:c.*125T= ENSP00000357461.3:n.*125T=
NM_000748.2:c.*125T= NP_000739.1:n.*125T=
XM_017000180.2:c.*125T= XP_016855669.1:n.*125T=
XR_001736952.2:n.1886T=
NM_000748.3:c.*125T= MANE Select NP_000739.1:n.*125T=