Canonical Allele Identifier: CA1335317619

Gene: CHRNG

Linked Data

• dbSNP Id: rs1692052870

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232543165A>G , CM000664.2:g.232543165A>G	GRCh38
NC_000002.11:g.233407875A>G , CM000664.1:g.233407875A>G	GRCh37
NC_000002.10:g.233116119A>G	NCBI36
NG_012954.1:g.8439A>G
NG_012954.2:g.8474A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000651502.1:c.805+83A>G MANE Select	ENSP00000498757.1:n.805+83A>G
ENST00000389492.3:c.649+83A>G	ENSP00000374143.3:n.649+83A>G
ENST00000389494.7:c.805+83A>G	ENSP00000374145.3:n.805+83A>G
NM_005199.4:c.805+83A>G	NP_005190.4:n.805+83A>G
NM_005199.5:c.805+83A>G MANE Select	NP_005190.4:n.805+83A>G