Canonical Allele Identifier: CA1335312163
Gene: CHRNG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232539780G= , CM000664.2:g.232539780G= GRCh38
NC_000002.11:g.233404490G= , CM000664.1:g.233404490G= GRCh37
NC_000002.10:g.233112734G= NCBI36
NG_012954.1:g.5054G=
NG_012954.2:g.5089G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.33G= MANE Select ENSP00000498757.1:p.Leu11=
ENST00000389492.3:c.33G= ENSP00000374143.3:p.Leu11=
ENST00000389494.7:c.33G= ENSP00000374145.3:p.Leu11=
ENST00000485094.1:n.54G=
NM_005199.4:c.33G= NP_005190.4:p.Leu11=
NM_005199.5:c.33G= MANE Select NP_005190.4:p.Leu11=