Canonical Allele Identifier: CA2648173577
Gene: CHRNB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154576250A>G , CM000663.2:g.154576250A>G GRCh38
NC_000001.10:g.154548726A>G , CM000663.1:g.154548726A>G GRCh37
NC_000001.9:g.152815350A>G NCBI36
NG_008027.1:g.13470A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000368476.4:c.*318A>G MANE Select ENSP00000357461.3:n.*318A>G
ENST00000636034.1:c.1505+322A>G ENSP00000489703.1:n.1505+322A>G
ENST00000637900.1:c.*318A>G ENSP00000490474.1:n.*318A>G
ENST00000368476.3:c.*318A>G ENSP00000357461.3:n.*318A>G
NM_000748.2:c.*318A>G NP_000739.1:n.*318A>G
XM_017000180.2:c.*318A>G XP_016855669.1:n.*318A>G
XR_001736952.2:n.2079A>G
NM_000748.3:c.*318A>G MANE Select NP_000739.1:n.*318A>G