Canonical Allele Identifier: CA1335316837

Gene: CHRNG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232541638G= , CM000664.2:g.232541638G=	GRCh38
NC_000002.11:g.233406348G= , CM000664.1:g.233406348G=	GRCh37
NC_000002.10:g.233114592G=	NCBI36
NG_012954.1:g.6912G=
NG_012954.2:g.6947G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.506+109G= MANE Select	ENSP00000498757.1:n.506+109G=
ENST00000389492.3:c.351-785G=	ENSP00000374143.3:n.351-785G=
ENST00000389494.7:c.506+109G=	ENSP00000374145.3:n.506+109G=
ENST00000485094.1:n.636G=
NM_005199.4:c.506+109G=	NP_005190.4:n.506+109G=
NM_005199.5:c.506+109G= MANE Select	NP_005190.4:n.506+109G=