Canonical Allele Identifier: CA1335317524

Gene: CHRNG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232542993G= , CM000664.2:g.232542993G=	GRCh38
NC_000002.11:g.233407703G= , CM000664.1:g.233407703G=	GRCh37
NC_000002.10:g.233115947G=	NCBI36
NG_012954.1:g.8267G=
NG_012954.2:g.8302G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000651502.1:c.716G= MANE Select	ENSP00000498757.1:p.Arg239=
ENST00000389492.3:c.560G=	ENSP00000374143.3:p.Arg187=
ENST00000389494.7:c.716G=	ENSP00000374145.3:p.Arg239=
NM_005199.4:c.716G=	NP_005190.4:p.Arg239=
NM_005199.5:c.716G= MANE Select	NP_005190.4:p.Arg239=