Canonical Allele Identifier: CA351009098
Gene: CHRNG HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.454A>T MANE Select ENSP00000498757.1:p.Ile152Phe
ENST00000389492.3:c.350+766A>T ENSP00000374143.3:n.350+766A>T
ENST00000389494.7:c.454A>T ENSP00000374145.3:p.Ile152Phe
ENST00000485094.1:n.475A>T
NM_005199.4:c.454A>T NP_005190.4:p.Ile152Phe
NM_005199.5:c.454A>T MANE Select NP_005190.4:p.Ile152Phe