Canonical Allele Identifier: CA421230971
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2806947
ClinVar RCV Id: RCV003746932
MyVariant Identifiers: chr1:g.154544025C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571549C>T , CM000663.2:g.154571549C>T GRCh38
NC_000001.10:g.154544025C>T , CM000663.1:g.154544025C>T GRCh37
NC_000001.9:g.152810649C>T NCBI36
NG_008027.1:g.8769C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.726C>T MANE Select ENSP00000357461.3:p.Ile242=
ENST00000636034.1:c.726C>T ENSP00000489703.1:p.Ile242=
ENST00000637900.1:c.732C>T ENSP00000490474.1:p.Ile244=
ENST00000368476.3:c.726C>T ENSP00000357461.3:p.Ile242=
NM_000748.2:c.726C>T NP_000739.1:p.Ile242=
XM_017000180.2:c.216C>T XP_016855669.1:p.Ile72=
XR_001736952.2:n.978C>T
NM_000748.3:c.726C>T MANE Select NP_000739.1:p.Ile242=