Canonical Allele Identifier: CA342631079
Gene: CHRNB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571728T>G , CM000663.2:g.154571728T>G GRCh38
NC_000001.10:g.154544204T>G , CM000663.1:g.154544204T>G GRCh37
NC_000001.9:g.152810828T>G NCBI36
NG_008027.1:g.8948T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.905T>G MANE Select ENSP00000357461.3:p.Met302Arg
ENST00000636034.1:c.905T>G ENSP00000489703.1:p.Met302Arg
ENST00000637900.1:c.911T>G ENSP00000490474.1:p.Met304Arg
ENST00000368476.3:c.905T>G ENSP00000357461.3:p.Met302Arg
NM_000748.2:c.905T>G NP_000739.1:p.Met302Arg
XM_017000180.2:c.395T>G XP_016855669.1:p.Met132Arg
XR_001736952.2:n.1157T>G
NM_000748.3:c.905T>G MANE Select NP_000739.1:p.Met302Arg