Canonical Allele Identifier: CA1335312302
Gene: CHRNG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232540004G= , CM000664.2:g.232540004G= GRCh38
NC_000002.11:g.233404714G= , CM000664.1:g.233404714G= GRCh37
NC_000002.10:g.233112958G= NCBI36
NG_012954.1:g.5278G=
NG_012954.2:g.5313G=

Transcript Alleles

HGVS Amino-acid change
ENST00000651502.1:c.68G= MANE Select ENSP00000498757.1:p.Arg23=
ENST00000389492.3:c.68G= ENSP00000374143.3:p.Arg23=
ENST00000389494.7:c.68G= ENSP00000374145.3:p.Arg23=
ENST00000485094.1:n.89G=
NM_005199.4:c.68G= NP_005190.4:p.Arg23=
NM_005199.5:c.68G= MANE Select NP_005190.4:p.Arg23=