Canonical Allele Identifier: CA351009041
Gene: CHRNG HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.448T>C MANE Select ENSP00000498757.1:p.Cys150Arg
ENST00000389492.3:c.350+760T>C ENSP00000374143.3:n.350+760T>C
ENST00000389494.7:c.448T>C ENSP00000374145.3:p.Cys150Arg
ENST00000485094.1:n.469T>C
NM_005199.4:c.448T>C NP_005190.4:p.Cys150Arg
NM_005199.5:c.448T>C MANE Select NP_005190.4:p.Cys150Arg