Canonical Allele Identifier: CA1335316767

Gene: CHRNG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232541482A= , CM000664.2:g.232541482A=	GRCh38
NC_000002.11:g.233406192A= , CM000664.1:g.233406192A=	GRCh37
NC_000002.10:g.233114436A=	NCBI36
NG_012954.1:g.6756A=
NG_012954.2:g.6791A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.459A= MANE Select	ENSP00000498757.1:p.Ser153=
ENST00000389492.3:c.350+771A=	ENSP00000374143.3:n.350+771A=
ENST00000389494.7:c.459A=	ENSP00000374145.3:p.Ser153=
ENST00000485094.1:n.480A=
NM_005199.4:c.459A=	NP_005190.4:p.Ser153=
NM_005199.5:c.459A= MANE Select	NP_005190.4:p.Ser153=