Canonical Allele Identifier: CA1335316764

Gene: CHRNG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232541476T= , CM000664.2:g.232541476T=	GRCh38
NC_000002.11:g.233406186T= , CM000664.1:g.233406186T=	GRCh37
NC_000002.10:g.233114430T=	NCBI36
NG_012954.1:g.6750T=
NG_012954.2:g.6785T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.453T= MANE Select	ENSP00000498757.1:p.Ser151=
ENST00000389492.3:c.350+765T=	ENSP00000374143.3:n.350+765T=
ENST00000389494.7:c.453T=	ENSP00000374145.3:p.Ser151=
ENST00000485094.1:n.474T=
NM_005199.4:c.453T=	NP_005190.4:p.Ser151=
NM_005199.5:c.453T= MANE Select	NP_005190.4:p.Ser151=