Canonical Allele Identifier: CA1335317527

Gene: CHRNG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232542999C= , CM000664.2:g.232542999C=	GRCh38
NC_000002.11:g.233407709C= , CM000664.1:g.233407709C=	GRCh37
NC_000002.10:g.233115953C=	NCBI36
NG_012954.1:g.8273C=
NG_012954.2:g.8308C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000651502.1:c.722C= MANE Select	ENSP00000498757.1:p.Pro241=
ENST00000389492.3:c.566C=	ENSP00000374143.3:p.Pro189=
ENST00000389494.7:c.722C=	ENSP00000374145.3:p.Pro241=
NM_005199.4:c.722C=	NP_005190.4:p.Pro241=
NM_005199.5:c.722C= MANE Select	NP_005190.4:p.Pro241=