Canonical Allele Identifier: CA342631005
Gene: CHRNB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571694T>G , CM000663.2:g.154571694T>G GRCh38
NC_000001.10:g.154544170T>G , CM000663.1:g.154544170T>G GRCh37
NC_000001.9:g.152810794T>G NCBI36
NG_008027.1:g.8914T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.871T>G MANE Select ENSP00000357461.3:p.Ser291Ala
ENST00000636034.1:c.871T>G ENSP00000489703.1:p.Ser291Ala
ENST00000637900.1:c.877T>G ENSP00000490474.1:p.Ser293Ala
ENST00000368476.3:c.871T>G ENSP00000357461.3:p.Ser291Ala
NM_000748.2:c.871T>G NP_000739.1:p.Ser291Ala
XM_017000180.2:c.361T>G XP_016855669.1:p.Ser121Ala
XR_001736952.2:n.1123T>G
NM_000748.3:c.871T>G MANE Select NP_000739.1:p.Ser291Ala