Canonical Allele Identifier: CA2577278058

Gene: CHRNG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232539929C>G , CM000664.2:g.232539929C>G	GRCh38
NC_000002.11:g.233404639C>G , CM000664.1:g.233404639C>G	GRCh37
NC_000002.10:g.233112883C>G	NCBI36
NG_012954.1:g.5203C>G
NG_012954.2:g.5238C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.56-63C>G MANE Select	ENSP00000498757.1:n.56-63C>G
ENST00000389492.3:c.56-63C>G	ENSP00000374143.3:n.56-63C>G
ENST00000389494.7:c.56-63C>G	ENSP00000374145.3:n.56-63C>G
ENST00000485094.1:n.77-63C>G
NM_005199.4:c.56-63C>G	NP_005190.4:n.56-63C>G
NM_005199.5:c.56-63C>G MANE Select	NP_005190.4:n.56-63C>G