Canonical Allele Identifier: CA1335316839

Gene: CHRNG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232541654T= , CM000664.2:g.232541654T=	GRCh38
NC_000002.11:g.233406364T= , CM000664.1:g.233406364T=	GRCh37
NC_000002.10:g.233114608T=	NCBI36
NG_012954.1:g.6928T=
NG_012954.2:g.6963T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.506+125T= MANE Select	ENSP00000498757.1:n.506+125T=
ENST00000389492.3:c.351-769T=	ENSP00000374143.3:n.351-769T=
ENST00000389494.7:c.506+125T=	ENSP00000374145.3:n.506+125T=
ENST00000485094.1:n.652T=
NM_005199.4:c.506+125T=	NP_005190.4:n.506+125T=
NM_005199.5:c.506+125T= MANE Select	NP_005190.4:n.506+125T=