Canonical Allele Identifier: CA2577278061

Gene: CHRNG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232539933G>T , CM000664.2:g.232539933G>T	GRCh38
NC_000002.11:g.233404643G>T , CM000664.1:g.233404643G>T	GRCh37
NC_000002.10:g.233112887G>T	NCBI36
NG_012954.1:g.5207G>T
NG_012954.2:g.5242G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.56-59G>T MANE Select	ENSP00000498757.1:n.56-59G>T
ENST00000389492.3:c.56-59G>T	ENSP00000374143.3:n.56-59G>T
ENST00000389494.7:c.56-59G>T	ENSP00000374145.3:n.56-59G>T
ENST00000485094.1:n.77-59G>T
NM_005199.4:c.56-59G>T	NP_005190.4:n.56-59G>T
NM_005199.5:c.56-59G>T MANE Select	NP_005190.4:n.56-59G>T