Canonical Allele Identifier: CA2746189328
Gene: CHRNB2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154576075T>A , CM000663.2:g.154576075T>A GRCh38
NC_000001.10:g.154548551T>A , CM000663.1:g.154548551T>A GRCh37
NC_000001.9:g.152815175T>A NCBI36
NG_008027.1:g.13295T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.*143T>A MANE Select ENSP00000357461.3:n.*143T>A
ENST00000636034.1:c.1505+147T>A ENSP00000489703.1:n.1505+147T>A
ENST00000637900.1:c.*143T>A ENSP00000490474.1:n.*143T>A
ENST00000368476.3:c.*143T>A ENSP00000357461.3:n.*143T>A
NM_000748.2:c.*143T>A NP_000739.1:n.*143T>A
XM_017000180.2:c.*143T>A XP_016855669.1:n.*143T>A
XR_001736952.2:n.1904T>A
NM_000748.3:c.*143T>A MANE Select NP_000739.1:n.*143T>A
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