Canonical Allele Identifier: CA66968790
Gene: CHRNG HGNC NCBI

Linked Data

dbSNP Id: rs578137720
gnomAD v3: 2-232543179-C-A
gnomAD v4: 2-232543179-C-A
MyVariant Identifiers: chr2:g.233407889C>A (hg19) chr2:g.232543179C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232543179C>A , CM000664.2:g.232543179C>A GRCh38
NC_000002.11:g.233407889C>A , CM000664.1:g.233407889C>A GRCh37
NC_000002.10:g.233116133C>A NCBI36
NG_012954.1:g.8453C>A
NG_012954.2:g.8488C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000651502.1:c.806-96C>A MANE Select ENSP00000498757.1:n.806-96C>A
ENST00000389492.3:c.650-96C>A ENSP00000374143.3:n.650-96C>A
ENST00000389494.7:c.806-96C>A ENSP00000374145.3:n.806-96C>A
NM_005199.4:c.806-96C>A NP_005190.4:n.806-96C>A
NM_005199.5:c.806-96C>A MANE Select NP_005190.4:n.806-96C>A
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