Canonical Allele Identifier: CA1130629
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 377680
dbSNP Id: rs71651693

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154569506C>T , CM000663.2:g.154569506C>T GRCh38
NC_000001.10:g.154541982C>T , CM000663.1:g.154541982C>T GRCh37
NC_000001.9:g.152808606C>T NCBI36
NG_008027.1:g.6726C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000368476.4:c.109C>T MANE Select ENSP00000357461.3:p.Leu37=
ENST00000636034.1:c.109C>T ENSP00000489703.1:p.Leu37=
ENST00000637900.1:c.109C>T ENSP00000490474.1:p.Leu37=
ENST00000368476.3:c.109C>T ENSP00000357461.3:p.Leu37=
NM_000748.2:c.109C>T NP_000739.1:p.Leu37=
XM_017000180.2:c.-266C>T XP_016855669.1:n.-266C>T
XR_001736952.2:n.361C>T
NM_000748.3:c.109C>T MANE Select NP_000739.1:p.Leu37=