Canonical Allele Identifier: CA2480927351
Gene: CHRNB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154576256_154576267delinsCCAGGAAGGGGA , CM000663.2:g.154576256_154576267delinsCCAGGAAGGGGA GRCh38
NC_000001.10:g.154548732_154548743delinsCCAGGAAGGGGA , CM000663.1:g.154548732_154548743delinsCCAGGAAGGGGA GRCh37
NC_000001.9:g.152815356_152815367delinsCCAGGAAGGGGA NCBI36
NG_008027.1:g.13476_13487delinsCCAGGAAGGGGA

Transcript Alleles

HGVS Amino-acid change
ENST00000368476.4:c.*324_*335delinsCCAGGAAGGGGA MANE Select ENSP00000357461.3:n.*324_*335delinsCCAGGA...
ENST00000636034.1:c.1505+328_1505+339delinsCCAGGAAGGGGA ENSP00000489703.1:n.1505+328_1505+339deli...
ENST00000637900.1:c.*324_*335delinsCCAGGAAGGGGA ENSP00000490474.1:n.*324_*335delinsCCAGGA...
ENST00000368476.3:c.*324_*335delinsCCAGGAAGGGGA ENSP00000357461.3:n.*324_*335delinsCCAGGA...
NM_000748.2:c.*324_*335delinsCCAGGAAGGGGA NP_000739.1:n.*324_*335delinsCCAGGAAGGGGA...
XM_017000180.2:c.*324_*335delinsCCAGGAAGGGGA XP_016855669.1:n.*324_*335delinsCCAGGAAGG...
XR_001736952.2:n.2085_2096delinsCCAGGAAGGGGA
NM_000748.3:c.*324_*335delinsCCAGGAAGGGGA MANE Select NP_000739.1:n.*324_*335delinsCCAGGAAGGGGA...