Canonical Allele Identifier: CA342630994
Gene: CHRNB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154571688C>G , CM000663.2:g.154571688C>G GRCh38
NC_000001.10:g.154544164C>G , CM000663.1:g.154544164C>G GRCh37
NC_000001.9:g.152810788C>G NCBI36
NG_008027.1:g.8908C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368476.4:c.865C>G MANE Select ENSP00000357461.3:p.Pro289Ala
ENST00000636034.1:c.865C>G ENSP00000489703.1:p.Pro289Ala
ENST00000637900.1:c.871C>G ENSP00000490474.1:p.Pro291Ala
ENST00000368476.3:c.865C>G ENSP00000357461.3:p.Pro289Ala
NM_000748.2:c.865C>G NP_000739.1:p.Pro289Ala
XM_017000180.2:c.355C>G XP_016855669.1:p.Pro119Ala
XR_001736952.2:n.1117C>G
NM_000748.3:c.865C>G MANE Select NP_000739.1:p.Pro289Ala