Canonical Allele Identifier: CA2754656888

Gene: CHRNG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232541590G>C , CM000664.2:g.232541590G>C	GRCh38
NC_000002.11:g.233406300G>C , CM000664.1:g.233406300G>C	GRCh37
NC_000002.10:g.233114544G>C	NCBI36
NG_012954.1:g.6864G>C
NG_012954.2:g.6899G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.506+61G>C MANE Select	ENSP00000498757.1:n.506+61G>C
ENST00000389492.3:c.351-833G>C	ENSP00000374143.3:n.351-833G>C
ENST00000389494.7:c.506+61G>C	ENSP00000374145.3:n.506+61G>C
ENST00000485094.1:n.588G>C
NM_005199.4:c.506+61G>C	NP_005190.4:n.506+61G>C
NM_005199.5:c.506+61G>C MANE Select	NP_005190.4:n.506+61G>C