Canonical Allele Identifier: CA2663626070
Gene: CHRNG HGNC NCBI

Linked Data

dbSNP Id: rs2106221833
gnomAD v4: 2-232543192-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232543192A>G , CM000664.2:g.232543192A>G GRCh38
NC_000002.11:g.233407902A>G , CM000664.1:g.233407902A>G GRCh37
NC_000002.10:g.233116146A>G NCBI36
NG_012954.1:g.8466A>G
NG_012954.2:g.8501A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.806-83A>G MANE Select ENSP00000498757.1:n.806-83A>G
ENST00000389492.3:c.650-83A>G ENSP00000374143.3:n.650-83A>G
ENST00000389494.7:c.806-83A>G ENSP00000374145.3:n.806-83A>G
NM_005199.4:c.806-83A>G NP_005190.4:n.806-83A>G
NM_005199.5:c.806-83A>G MANE Select NP_005190.4:n.806-83A>G
Search 100 bp 5'
Search 100 bp 3'