Canonical Allele Identifier: CA1335316771

Gene: CHRNG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232541494C= , CM000664.2:g.232541494C=	GRCh38
NC_000002.11:g.233406204C= , CM000664.1:g.233406204C=	GRCh37
NC_000002.10:g.233114448C=	NCBI36
NG_012954.1:g.6768C=
NG_012954.2:g.6803C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.471C= MANE Select	ENSP00000498757.1:p.Phe157=
ENST00000389492.3:c.350+783C=	ENSP00000374143.3:n.350+783C=
ENST00000389494.7:c.471C=	ENSP00000374145.3:p.Phe157=
ENST00000485094.1:n.492C=
NM_005199.4:c.471C=	NP_005190.4:p.Phe157=
NM_005199.5:c.471C= MANE Select	NP_005190.4:p.Phe157=