Canonical Allele Identifier: CA1148447189
Gene: CHRNB2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571172T= , CM000663.2:g.154571172T= GRCh38
NC_000001.10:g.154543648T= , CM000663.1:g.154543648T= GRCh37
NC_000001.9:g.152810272T= NCBI36
NG_008027.1:g.8392T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.366-17T= MANE Select ENSP00000357461.3:n.366-17T=
ENST00000636034.1:c.366-17T= ENSP00000489703.1:n.366-17T=
ENST00000637900.1:c.372-17T= ENSP00000490474.1:n.372-17T=
ENST00000368476.3:c.366-17T= ENSP00000357461.3:n.366-17T=
NM_000748.2:c.366-17T= NP_000739.1:n.366-17T=
XM_017000180.2:c.-9-153T= XP_016855669.1:n.-9-153T=
XR_001736952.2:n.618-17T=
NM_000748.3:c.366-17T= MANE Select NP_000739.1:n.366-17T=
Search 100 bp 5'
Search 100 bp 3'