Canonical Allele Identifier: CA351008976
Gene: CHRNG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232541460T>G , CM000664.2:g.232541460T>G GRCh38
NC_000002.11:g.233406170T>G , CM000664.1:g.233406170T>G GRCh37
NC_000002.10:g.233114414T>G NCBI36
NG_012954.1:g.6734T>G
NG_012954.2:g.6769T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.437T>G MANE Select ENSP00000498757.1:p.Phe146Cys
ENST00000389492.3:c.350+749T>G ENSP00000374143.3:n.350+749T>G
ENST00000389494.7:c.437T>G ENSP00000374145.3:p.Phe146Cys
ENST00000485094.1:n.458T>G
NM_005199.4:c.437T>G NP_005190.4:p.Phe146Cys
NM_005199.5:c.437T>G MANE Select NP_005190.4:p.Phe146Cys