Canonical Allele Identifier: CA1335316741

Gene: CHRNG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232541433G= , CM000664.2:g.232541433G=	GRCh38
NC_000002.11:g.233406143G= , CM000664.1:g.233406143G=	GRCh37
NC_000002.10:g.233114387G=	NCBI36
NG_012954.1:g.6707G=
NG_012954.2:g.6742G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.410G= MANE Select	ENSP00000498757.1:p.Cys137=
ENST00000389492.3:c.350+722G=	ENSP00000374143.3:n.350+722G=
ENST00000389494.7:c.410G=	ENSP00000374145.3:p.Cys137=
ENST00000485094.1:n.431G=
NM_005199.4:c.410G=	NP_005190.4:p.Cys137=
NM_005199.5:c.410G= MANE Select	NP_005190.4:p.Cys137=