Canonical Allele Identifier: CA2648170624
Gene: CHRNB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571695_154571707del , CM000663.2:g.154571695_154571707del GRCh38
NC_000001.10:g.154544171_154544183del , CM000663.1:g.154544171_154544183del GRCh37
NC_000001.9:g.152810795_152810807del NCBI36
NG_008027.1:g.8915_8927del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.872_884del MANE Select ENSP00000357461.3:p.Ser291CysfsTer?
ENST00000636034.1:c.872_884del ENSP00000489703.1:p.Ser291CysfsTer?
ENST00000637900.1:c.878_890del ENSP00000490474.1:p.Ser293CysfsTer?
ENST00000368476.3:c.872_884del ENSP00000357461.3:p.Ser291CysfsTer?
NM_000748.2:c.872_884del NP_000739.1:p.Ser291CysfsTer?
XM_017000180.2:c.362_374del XP_016855669.1:p.Ser121CysfsTer?
XR_001736952.2:n.1124_1136del
NM_000748.3:c.872_884del MANE Select NP_000739.1:p.Ser291CysfsTer?