Canonical Allele Identifier: CA2480927262
Gene: CHRNB2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154576066A= , CM000663.2:g.154576066A= GRCh38
NC_000001.10:g.154548542A= , CM000663.1:g.154548542A= GRCh37
NC_000001.9:g.152815166A= NCBI36
NG_008027.1:g.13286A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.*134A= MANE Select ENSP00000357461.3:n.*134A=
ENST00000636034.1:c.1505+138A= ENSP00000489703.1:n.1505+138A=
ENST00000637900.1:c.*134A= ENSP00000490474.1:n.*134A=
ENST00000368476.3:c.*134A= ENSP00000357461.3:n.*134A=
NM_000748.2:c.*134A= NP_000739.1:n.*134A=
XM_017000180.2:c.*134A= XP_016855669.1:n.*134A=
XR_001736952.2:n.1895A=
NM_000748.3:c.*134A= MANE Select NP_000739.1:n.*134A=
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