Canonical Allele Identifier: CA2648173605
Gene: CHRNB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154576255G>T , CM000663.2:g.154576255G>T GRCh38
NC_000001.10:g.154548731G>T , CM000663.1:g.154548731G>T GRCh37
NC_000001.9:g.152815355G>T NCBI36
NG_008027.1:g.13475G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000368476.4:c.*323G>T MANE Select ENSP00000357461.3:n.*323G>T
ENST00000636034.1:c.1505+327G>T ENSP00000489703.1:n.1505+327G>T
ENST00000637900.1:c.*323G>T ENSP00000490474.1:n.*323G>T
ENST00000368476.3:c.*323G>T ENSP00000357461.3:n.*323G>T
NM_000748.2:c.*323G>T NP_000739.1:n.*323G>T
XM_017000180.2:c.*323G>T XP_016855669.1:n.*323G>T
XR_001736952.2:n.2084G>T
NM_000748.3:c.*323G>T MANE Select NP_000739.1:n.*323G>T