Canonical Allele Identifier: CA1335312239
Gene: CHRNG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232539912A= , CM000664.2:g.232539912A= GRCh38
NC_000002.11:g.233404622A= , CM000664.1:g.233404622A= GRCh37
NC_000002.10:g.233112866A= NCBI36
NG_012954.1:g.5186A=
NG_012954.2:g.5221A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.56-80A= MANE Select ENSP00000498757.1:n.56-80A=
ENST00000389492.3:c.56-80A= ENSP00000374143.3:n.56-80A=
ENST00000389494.7:c.56-80A= ENSP00000374145.3:n.56-80A=
ENST00000485094.1:n.77-80A=
NM_005199.4:c.56-80A= NP_005190.4:n.56-80A=
NM_005199.5:c.56-80A= MANE Select NP_005190.4:n.56-80A=