Canonical Allele Identifier: CA1143426688
Gene: CHRNB2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154576175G= , CM000663.2:g.154576175G= GRCh38
NC_000001.10:g.154548651G= , CM000663.1:g.154548651G= GRCh37
NC_000001.9:g.152815275G= NCBI36
NG_008027.1:g.13395G=

Transcript Alleles

HGVS Amino-acid change
ENST00000368476.4:c.*243G= MANE Select ENSP00000357461.3:n.*243G=
ENST00000636034.1:c.1505+247G= ENSP00000489703.1:n.1505+247G=
ENST00000637900.1:c.*243G= ENSP00000490474.1:n.*243G=
ENST00000368476.3:c.*243G= ENSP00000357461.3:n.*243G=
NM_000748.2:c.*243G= NP_000739.1:n.*243G=
XM_017000180.2:c.*243G= XP_016855669.1:n.*243G=
XR_001736952.2:n.2004G=
NM_000748.3:c.*243G= MANE Select NP_000739.1:n.*243G=
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