Canonical Allele Identifier: CA66968806
Gene: CHRNG HGNC NCBI

Linked Data

dbSNP Id: rs566102476
gnomAD v2: 2-233407904-C-A
gnomAD v3: 2-232543194-C-A
gnomAD v4: 2-232543194-C-A
MyVariant Identifiers: chr2:g.233407904C>A (hg19) chr2:g.232543194C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232543194C>A , CM000664.2:g.232543194C>A GRCh38
NC_000002.11:g.233407904C>A , CM000664.1:g.233407904C>A GRCh37
NC_000002.10:g.233116148C>A NCBI36
NG_012954.1:g.8468C>A
NG_012954.2:g.8503C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000651502.1:c.806-81C>A MANE Select ENSP00000498757.1:n.806-81C>A
ENST00000389492.3:c.650-81C>A ENSP00000374143.3:n.650-81C>A
ENST00000389494.7:c.806-81C>A ENSP00000374145.3:n.806-81C>A
NM_005199.4:c.806-81C>A NP_005190.4:n.806-81C>A
NM_005199.5:c.806-81C>A MANE Select NP_005190.4:n.806-81C>A
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