Canonical Allele Identifier: CA647660271
Gene: CHRNG HGNC NCBI

Linked Data

COSMIC: COSN8868001
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232543167T>A , CM000664.2:g.232543167T>A GRCh38
NC_000002.11:g.233407877T>A , CM000664.1:g.233407877T>A GRCh37
NC_000002.10:g.233116121T>A NCBI36
NG_012954.1:g.8441T>A
NG_012954.2:g.8476T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000651502.1:c.805+85T>A MANE Select ENSP00000498757.1:n.805+85T>A
ENST00000389492.3:c.649+85T>A ENSP00000374143.3:n.649+85T>A
ENST00000389494.7:c.805+85T>A ENSP00000374145.3:n.805+85T>A
NM_005199.4:c.805+85T>A NP_005190.4:n.805+85T>A
NM_005199.5:c.805+85T>A MANE Select NP_005190.4:n.805+85T>A
Search 100 bp 5'
Search 100 bp 3'