Canonical Allele Identifier: CA30834309
Gene: CHRNB2 HGNC NCBI

Linked Data

dbSNP Id: rs868808487
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571469_154571470delinsTT , CM000663.2:g.154571469_154571470delinsTT GRCh38
NC_000001.10:g.154543945_154543946delinsTT , CM000663.1:g.154543945_154543946delinsTT GRCh37
NC_000001.9:g.152810569_152810570delinsTT NCBI36
NG_008027.1:g.8689_8690delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.646_647delinsTT MANE Select ENSP00000357461.3:p.Pro216Phe
ENST00000636034.1:c.646_647delinsTT ENSP00000489703.1:p.Pro216Phe
ENST00000637900.1:c.652_653delinsTT ENSP00000490474.1:p.Pro218Phe
ENST00000368476.3:c.646_647delinsTT ENSP00000357461.3:p.Pro216Phe
NM_000748.2:c.646_647delinsTT NP_000739.1:p.Pro216Phe
XM_017000180.2:c.136_137delinsTT XP_016855669.1:p.Pro46Phe
XR_001736952.2:n.898_899delinsTT
NM_000748.3:c.646_647delinsTT MANE Select NP_000739.1:p.Pro216Phe
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