Canonical Allele Identifier: CA351009037
Gene: CHRNG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232541471T>A , CM000664.2:g.232541471T>A GRCh38
NC_000002.11:g.233406181T>A , CM000664.1:g.233406181T>A GRCh37
NC_000002.10:g.233114425T>A NCBI36
NG_012954.1:g.6745T>A
NG_012954.2:g.6780T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.448T>A MANE Select ENSP00000498757.1:p.Cys150Ser
ENST00000389492.3:c.350+760T>A ENSP00000374143.3:n.350+760T>A
ENST00000389494.7:c.448T>A ENSP00000374145.3:p.Cys150Ser
ENST00000485094.1:n.469T>A
NM_005199.4:c.448T>A NP_005190.4:p.Cys150Ser
NM_005199.5:c.448T>A MANE Select NP_005190.4:p.Cys150Ser