Canonical Allele Identifier: CA2754656884

Gene: CHRNG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232541546G>T , CM000664.2:g.232541546G>T	GRCh38
NC_000002.11:g.233406256G>T , CM000664.1:g.233406256G>T	GRCh37
NC_000002.10:g.233114500G>T	NCBI36
NG_012954.1:g.6820G>T
NG_012954.2:g.6855G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.506+17G>T MANE Select	ENSP00000498757.1:n.506+17G>T
ENST00000389492.3:c.350+835G>T	ENSP00000374143.3:n.350+835G>T
ENST00000389494.7:c.506+17G>T	ENSP00000374145.3:n.506+17G>T
ENST00000485094.1:n.544G>T
NM_005199.4:c.506+17G>T	NP_005190.4:n.506+17G>T
NM_005199.5:c.506+17G>T MANE Select	NP_005190.4:n.506+17G>T