Canonical Allele Identifier: CA342630246
Gene: CHRNB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571355T>C , CM000663.2:g.154571355T>C GRCh38
NC_000001.10:g.154543831T>C , CM000663.1:g.154543831T>C GRCh37
NC_000001.9:g.152810455T>C NCBI36
NG_008027.1:g.8575T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.532T>C MANE Select ENSP00000357461.3:p.Tyr178His
ENST00000636034.1:c.532T>C ENSP00000489703.1:p.Tyr178His
ENST00000637900.1:c.538T>C ENSP00000490474.1:p.Tyr180His
ENST00000368476.3:c.532T>C ENSP00000357461.3:p.Tyr178His
NM_000748.2:c.532T>C NP_000739.1:p.Tyr178His
XM_017000180.2:c.22T>C XP_016855669.1:p.Tyr8His
XR_001736952.2:n.784T>C
NM_000748.3:c.532T>C MANE Select NP_000739.1:p.Tyr178His