Canonical Allele Identifier: CA342630679
Gene: CHRNB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571535A>T , CM000663.2:g.154571535A>T GRCh38
NC_000001.10:g.154544011A>T , CM000663.1:g.154544011A>T GRCh37
NC_000001.9:g.152810635A>T NCBI36
NG_008027.1:g.8755A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.712A>T MANE Select ENSP00000357461.3:p.Thr238Ser
ENST00000636034.1:c.712A>T ENSP00000489703.1:p.Thr238Ser
ENST00000637900.1:c.718A>T ENSP00000490474.1:p.Thr240Ser
ENST00000368476.3:c.712A>T ENSP00000357461.3:p.Thr238Ser
NM_000748.2:c.712A>T NP_000739.1:p.Thr238Ser
XM_017000180.2:c.202A>T XP_016855669.1:p.Thr68Ser
XR_001736952.2:n.964A>T
NM_000748.3:c.712A>T MANE Select NP_000739.1:p.Thr238Ser