Canonical Allele Identifier: CA351009226
Gene: CHRNG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232541493T>A , CM000664.2:g.232541493T>A GRCh38
NC_000002.11:g.233406203T>A , CM000664.1:g.233406203T>A GRCh37
NC_000002.10:g.233114447T>A NCBI36
NG_012954.1:g.6767T>A
NG_012954.2:g.6802T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.470T>A MANE Select ENSP00000498757.1:p.Phe157Tyr
ENST00000389492.3:c.350+782T>A ENSP00000374143.3:n.350+782T>A
ENST00000389494.7:c.470T>A ENSP00000374145.3:p.Phe157Tyr
ENST00000485094.1:n.491T>A
NM_005199.4:c.470T>A NP_005190.4:p.Phe157Tyr
NM_005199.5:c.470T>A MANE Select NP_005190.4:p.Phe157Tyr