Canonical Allele Identifier: CA2663621506
Gene: CHRNG HGNC NCBI

Linked Data

gnomAD v4: 2-232539903-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232539903A>G , CM000664.2:g.232539903A>G GRCh38
NC_000002.11:g.233404613A>G , CM000664.1:g.233404613A>G GRCh37
NC_000002.10:g.233112857A>G NCBI36
NG_012954.1:g.5177A>G
NG_012954.2:g.5212A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.56-89A>G MANE Select ENSP00000498757.1:n.56-89A>G
ENST00000389492.3:c.56-89A>G ENSP00000374143.3:n.56-89A>G
ENST00000389494.7:c.56-89A>G ENSP00000374145.3:n.56-89A>G
ENST00000485094.1:n.77-89A>G
NM_005199.4:c.56-89A>G NP_005190.4:n.56-89A>G
NM_005199.5:c.56-89A>G MANE Select NP_005190.4:n.56-89A>G
Search 100 bp 5'
Search 100 bp 3'