Canonical Allele Identifier: CA2648173608
Gene: CHRNB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154576257del , CM000663.2:g.154576257del GRCh38
NC_000001.10:g.154548733del , CM000663.1:g.154548733del GRCh37
NC_000001.9:g.152815357del NCBI36
NG_008027.1:g.13477del

Transcript Alleles

HGVS Amino-acid change
ENST00000368476.4:c.*325del MANE Select ENSP00000357461.3:n.*325del
ENST00000636034.1:c.1505+329del ENSP00000489703.1:n.1505+329del
ENST00000637900.1:c.*325del ENSP00000490474.1:n.*325del
ENST00000368476.3:c.*325del ENSP00000357461.3:n.*325del
NM_000748.2:c.*325del NP_000739.1:n.*325del
XM_017000180.2:c.*325del XP_016855669.1:n.*325del
XR_001736952.2:n.2086del
NM_000748.3:c.*325del MANE Select NP_000739.1:n.*325del