Canonical Allele Identifier: CA351009029
Gene: CHRNG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232541469C>A , CM000664.2:g.232541469C>A GRCh38
NC_000002.11:g.233406179C>A , CM000664.1:g.233406179C>A GRCh37
NC_000002.10:g.233114423C>A NCBI36
NG_012954.1:g.6743C>A
NG_012954.2:g.6778C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.446C>A MANE Select ENSP00000498757.1:p.Ala149Asp
ENST00000389492.3:c.350+758C>A ENSP00000374143.3:n.350+758C>A
ENST00000389494.7:c.446C>A ENSP00000374145.3:p.Ala149Asp
ENST00000485094.1:n.467C>A
NM_005199.4:c.446C>A NP_005190.4:p.Ala149Asp
NM_005199.5:c.446C>A MANE Select NP_005190.4:p.Ala149Asp