Canonical Allele Identifier: CA2168491
Gene: CHRNG HGNC NCBI

Linked Data

dbSNP Id: rs764775222
ExAC: 2:233404711 G / A
gnomAD v2: 2-233404711-G-A
gnomAD v4: 2-232540001-G-A
MyVariant Identifiers: chr2:g.233404711G>A (hg19) chr2:g.232540001G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232540001G>A , CM000664.2:g.232540001G>A GRCh38
NC_000002.11:g.233404711G>A , CM000664.1:g.233404711G>A GRCh37
NC_000002.10:g.233112955G>A NCBI36
NG_012954.1:g.5275G>A
NG_012954.2:g.5310G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000651502.1:c.65G>A MANE Select ENSP00000498757.1:p.Gly22Asp
ENST00000389492.3:c.65G>A ENSP00000374143.3:p.Gly22Asp
ENST00000389494.7:c.65G>A ENSP00000374145.3:p.Gly22Asp
ENST00000485094.1:n.86G>A
NM_005199.4:c.65G>A NP_005190.4:p.Gly22Asp
NM_005199.5:c.65G>A MANE Select NP_005190.4:p.Gly22Asp
Search 100 bp 5'
Search 100 bp 3'