Canonical Allele Identifier: CA1335316754

Gene: CHRNG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232541456A= , CM000664.2:g.232541456A=	GRCh38
NC_000002.11:g.233406166A= , CM000664.1:g.233406166A=	GRCh37
NC_000002.10:g.233114410A=	NCBI36
NG_012954.1:g.6730A=
NG_012954.2:g.6765A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.433A= MANE Select	ENSP00000498757.1:p.Ile145=
ENST00000389492.3:c.350+745A=	ENSP00000374143.3:n.350+745A=
ENST00000389494.7:c.433A=	ENSP00000374145.3:p.Ile145=
ENST00000485094.1:n.454A=
NM_005199.4:c.433A=	NP_005190.4:p.Ile145=
NM_005199.5:c.433A= MANE Select	NP_005190.4:p.Ile145=