Canonical Allele Identifier: CA15091686
Gene: CHRNB2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2072660

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154576245T>C , CM000663.2:g.154576245T>C GRCh38
NC_000001.10:g.154548721T>C , CM000663.1:g.154548721T>C GRCh37
NC_000001.9:g.152815345T>C NCBI36
NG_008027.1:g.13465T>C

Transcript Alleles

HGVS Amino-acid change
NM_000748.2:c.*313T>C VV NP_000739.1:p.=
XM_017000180.2:c.*313T>C XP_016855669.1:p.=
XR_001736952.2:n.2074T>C
ENST00000368476.3:c.*313T>C ENSP00000357461.3:p.=