Canonical Allele Identifier: CA1335316779
Gene: CHRNG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232541511A= , CM000664.2:g.232541511A= GRCh38
NC_000002.11:g.233406221A= , CM000664.1:g.233406221A= GRCh37
NC_000002.10:g.233114465A= NCBI36
NG_012954.1:g.6785A=
NG_012954.2:g.6820A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.488A= MANE Select ENSP00000498757.1:p.Asn163=
ENST00000389492.3:c.350+800A= ENSP00000374143.3:n.350+800A=
ENST00000389494.7:c.488A= ENSP00000374145.3:p.Asn163=
ENST00000485094.1:n.509A=
NM_005199.4:c.488A= NP_005190.4:p.Asn163=
NM_005199.5:c.488A= MANE Select NP_005190.4:p.Asn163=