Canonical Allele Identifier: CA1335317145
Gene: CHRNG HGNC NCBI

Linked Data

dbSNP Id: rs1881492

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232542288T>A , CM000664.2:g.232542288T>A GRCh38
NC_000002.11:g.233406998T>A , CM000664.1:g.233406998T>A GRCh37
NC_000002.10:g.233115242T>A NCBI36
NG_012954.1:g.7562T>A
NG_012954.2:g.7597T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000651502.1:c.507-135T>A MANE Select ENSP00000498757.1:n.507-135T>A
ENST00000389492.3:c.351-135T>A ENSP00000374143.3:n.351-135T>A
ENST00000389494.7:c.507-135T>A ENSP00000374145.3:n.507-135T>A
NM_005199.4:c.507-135T>A NP_005190.4:n.507-135T>A
NM_005199.5:c.507-135T>A MANE Select NP_005190.4:n.507-135T>A