Canonical Allele Identifier: CA351009094
Gene: CHRNG HGNC NCBI

Linked Data

dbSNP Id: rs1692016733

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232541477A>G , CM000664.2:g.232541477A>G GRCh38
NC_000002.11:g.233406187A>G , CM000664.1:g.233406187A>G GRCh37
NC_000002.10:g.233114431A>G NCBI36
NG_012954.1:g.6751A>G
NG_012954.2:g.6786A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.454A>G MANE Select ENSP00000498757.1:p.Ile152Val
ENST00000389492.3:c.350+766A>G ENSP00000374143.3:n.350+766A>G
ENST00000389494.7:c.454A>G ENSP00000374145.3:p.Ile152Val
ENST00000485094.1:n.475A>G
NM_005199.4:c.454A>G NP_005190.4:p.Ile152Val
NM_005199.5:c.454A>G MANE Select NP_005190.4:p.Ile152Val