Canonical Allele Identifier: CA1335316817
Gene: CHRNG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232541592G= , CM000664.2:g.232541592G= GRCh38
NC_000002.11:g.233406302G= , CM000664.1:g.233406302G= GRCh37
NC_000002.10:g.233114546G= NCBI36
NG_012954.1:g.6866G=
NG_012954.2:g.6901G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.506+63G= MANE Select ENSP00000498757.1:n.506+63G=
ENST00000389492.3:c.351-831G= ENSP00000374143.3:n.351-831G=
ENST00000389494.7:c.506+63G= ENSP00000374145.3:n.506+63G=
ENST00000485094.1:n.590G=
NM_005199.4:c.506+63G= NP_005190.4:n.506+63G=
NM_005199.5:c.506+63G= MANE Select NP_005190.4:n.506+63G=