Canonical Allele Identifier: CA1144163639
Gene: CHRNB2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571169C= , CM000663.2:g.154571169C= GRCh38
NC_000001.10:g.154543645C= , CM000663.1:g.154543645C= GRCh37
NC_000001.9:g.152810269C= NCBI36
NG_008027.1:g.8389C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.366-20C= MANE Select ENSP00000357461.3:n.366-20C=
ENST00000636034.1:c.366-20C= ENSP00000489703.1:n.366-20C=
ENST00000637900.1:c.372-20C= ENSP00000490474.1:n.372-20C=
ENST00000368476.3:c.366-20C= ENSP00000357461.3:n.366-20C=
NM_000748.2:c.366-20C= NP_000739.1:n.366-20C=
XM_017000180.2:c.-9-156C= XP_016855669.1:n.-9-156C=
XR_001736952.2:n.618-20C=
NM_000748.3:c.366-20C= MANE Select NP_000739.1:n.366-20C=
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