Canonical Allele Identifier: CA2648173311
Gene: CHRNB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154576173_154576174del , CM000663.2:g.154576173_154576174del GRCh38
NC_000001.10:g.154548649_154548650del , CM000663.1:g.154548649_154548650del GRCh37
NC_000001.9:g.152815273_152815274del NCBI36
NG_008027.1:g.13393_13394del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.*241_*242del MANE Select ENSP00000357461.3:n.*241_*242del
ENST00000636034.1:c.1505+245_1505+246del ENSP00000489703.1:n.1505+245_1505+246del
ENST00000637900.1:c.*241_*242del ENSP00000490474.1:n.*241_*242del
ENST00000368476.3:c.*241_*242del ENSP00000357461.3:n.*241_*242del
NM_000748.2:c.*241_*242del NP_000739.1:n.*241_*242del
XM_017000180.2:c.*241_*242del XP_016855669.1:n.*241_*242del
XR_001736952.2:n.2002_2003del
NM_000748.3:c.*241_*242del MANE Select NP_000739.1:n.*241_*242del