Canonical Allele Identifier: CA2663621494
Gene: CHRNG HGNC NCBI

Linked Data

gnomAD v4: 2-232539899-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232539899A>C , CM000664.2:g.232539899A>C GRCh38
NC_000002.11:g.233404609A>C , CM000664.1:g.233404609A>C GRCh37
NC_000002.10:g.233112853A>C NCBI36
NG_012954.1:g.5173A>C
NG_012954.2:g.5208A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000651502.1:c.56-93A>C MANE Select ENSP00000498757.1:n.56-93A>C
ENST00000389492.3:c.56-93A>C ENSP00000374143.3:n.56-93A>C
ENST00000389494.7:c.56-93A>C ENSP00000374145.3:n.56-93A>C
ENST00000485094.1:n.77-93A>C
NM_005199.4:c.56-93A>C NP_005190.4:n.56-93A>C
NM_005199.5:c.56-93A>C MANE Select NP_005190.4:n.56-93A>C
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