Canonical Allele Identifier: CA2648172988
Gene: CHRNB2 HGNC NCBI

Linked Data

gnomAD v4: 1-154576062-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154576062C>A , CM000663.2:g.154576062C>A GRCh38
NC_000001.10:g.154548538C>A , CM000663.1:g.154548538C>A GRCh37
NC_000001.9:g.152815162C>A NCBI36
NG_008027.1:g.13282C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.*130C>A MANE Select ENSP00000357461.3:n.*130C>A
ENST00000636034.1:c.1505+134C>A ENSP00000489703.1:n.1505+134C>A
ENST00000637900.1:c.*130C>A ENSP00000490474.1:n.*130C>A
ENST00000368476.3:c.*130C>A ENSP00000357461.3:n.*130C>A
NM_000748.2:c.*130C>A NP_000739.1:n.*130C>A
XM_017000180.2:c.*130C>A XP_016855669.1:n.*130C>A
XR_001736952.2:n.1891C>A
NM_000748.3:c.*130C>A MANE Select NP_000739.1:n.*130C>A
Search 100 bp 5'
Search 100 bp 3'