Canonical Allele Identifier: CA1335316790

Gene: CHRNG

Linked Data

• dbSNP Id: rs1692018053

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232541542A>C , CM000664.2:g.232541542A>C	GRCh38
NC_000002.11:g.233406252A>C , CM000664.1:g.233406252A>C	GRCh37
NC_000002.10:g.233114496A>C	NCBI36
NG_012954.1:g.6816A>C
NG_012954.2:g.6851A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.506+13A>C MANE Select	ENSP00000498757.1:n.506+13A>C
ENST00000389492.3:c.350+831A>C	ENSP00000374143.3:n.350+831A>C
ENST00000389494.7:c.506+13A>C	ENSP00000374145.3:n.506+13A>C
ENST00000485094.1:n.540A>C
NM_005199.4:c.506+13A>C	NP_005190.4:n.506+13A>C
NM_005199.5:c.506+13A>C MANE Select	NP_005190.4:n.506+13A>C