Canonical Allele Identifier: CA1335316804

Gene: CHRNG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232541572A= , CM000664.2:g.232541572A=	GRCh38
NC_000002.11:g.233406282A= , CM000664.1:g.233406282A=	GRCh37
NC_000002.10:g.233114526A=	NCBI36
NG_012954.1:g.6846A=
NG_012954.2:g.6881A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.506+43A= MANE Select	ENSP00000498757.1:n.506+43A=
ENST00000389492.3:c.351-851A=	ENSP00000374143.3:n.351-851A=
ENST00000389494.7:c.506+43A=	ENSP00000374145.3:n.506+43A=
ENST00000485094.1:n.570A=
NM_005199.4:c.506+43A=	NP_005190.4:n.506+43A=
NM_005199.5:c.506+43A= MANE Select	NP_005190.4:n.506+43A=