Canonical Allele Identifier: CA342629350
Gene: CHRNB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 543530
ClinVar RCV Id: RCV000654322
dbSNP Id: rs1553204015

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154569551G>A , CM000663.2:g.154569551G>A GRCh38
NC_000001.10:g.154542027G>A , CM000663.1:g.154542027G>A GRCh37
NC_000001.9:g.152808651G>A NCBI36
NG_008027.1:g.6771G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.154G>A MANE Select ENSP00000357461.3:p.Gly52Ser
ENST00000636034.1:c.154G>A ENSP00000489703.1:p.Gly52Ser
ENST00000636695.1:c.24G>A
ENST00000637900.1:c.154G>A ENSP00000490474.1:p.Gly52Ser
ENST00000368476.3:c.154G>A ENSP00000357461.3:p.Gly52Ser
NM_000748.2:c.154G>A NP_000739.1:p.Gly52Ser
XM_017000180.2:c.-221G>A XP_016855669.1:n.-221G>A
XR_001736952.2:n.406G>A
NM_000748.3:c.154G>A MANE Select NP_000739.1:p.Gly52Ser