Canonical Allele Identifier: CA1007917959
Gene: CHRNB2 HGNC NCBI

Linked Data

dbSNP Id: rs1696274988

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154576244_154576245del , CM000663.2:g.154576244_154576245del GRCh38
NC_000001.10:g.154548720_154548721del , CM000663.1:g.154548720_154548721del GRCh37
NC_000001.9:g.152815344_152815345del NCBI36
NG_008027.1:g.13464_13465del

Transcript Alleles

HGVS Amino-acid change
ENST00000368476.4:c.*312_*313del MANE Select ENSP00000357461.3:n.*312_*313del
ENST00000636034.1:c.1505+316_1505+317del ENSP00000489703.1:n.1505+316_1505+317del
ENST00000637900.1:c.*312_*313del ENSP00000490474.1:n.*312_*313del
ENST00000368476.3:c.*312_*313del ENSP00000357461.3:n.*312_*313del
NM_000748.2:c.*312_*313del NP_000739.1:n.*312_*313del
XM_017000180.2:c.*312_*313del XP_016855669.1:n.*312_*313del
XR_001736952.2:n.2073_2074del
NM_000748.3:c.*312_*313del MANE Select NP_000739.1:n.*312_*313del