Canonical Allele Identifier: CA1335316769

Gene: CHRNG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232541490A= , CM000664.2:g.232541490A=	GRCh38
NC_000002.11:g.233406200A= , CM000664.1:g.233406200A=	GRCh37
NC_000002.10:g.233114444A=	NCBI36
NG_012954.1:g.6764A=
NG_012954.2:g.6799A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.467A= MANE Select	ENSP00000498757.1:p.Tyr156=
ENST00000389492.3:c.350+779A=	ENSP00000374143.3:n.350+779A=
ENST00000389494.7:c.467A=	ENSP00000374145.3:p.Tyr156=
ENST00000485094.1:n.488A=
NM_005199.4:c.467A=	NP_005190.4:p.Tyr156=
NM_005199.5:c.467A= MANE Select	NP_005190.4:p.Tyr156=