Canonical Allele Identifier: CA1335316843
Gene: CHRNG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232541661G= , CM000664.2:g.232541661G= GRCh38
NC_000002.11:g.233406371G= , CM000664.1:g.233406371G= GRCh37
NC_000002.10:g.233114615G= NCBI36
NG_012954.1:g.6935G=
NG_012954.2:g.6970G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.506+132G= MANE Select ENSP00000498757.1:n.506+132G=
ENST00000389492.3:c.351-762G= ENSP00000374143.3:n.351-762G=
ENST00000389494.7:c.506+132G= ENSP00000374145.3:n.506+132G=
ENST00000485094.1:n.659G=
NM_005199.4:c.506+132G= NP_005190.4:n.506+132G=
NM_005199.5:c.506+132G= MANE Select NP_005190.4:n.506+132G=