Canonical Allele Identifier: CA766142637
Gene: CHRNG HGNC NCBI

Linked Data

dbSNP Id: rs1407975605
gnomAD v3: 2-232541292-T-G
gnomAD v4: 2-232541292-T-G
MyVariant Identifiers: chr2:g.233406002T>G (hg19) chr2:g.232541292T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232541292T>G , CM000664.2:g.232541292T>G GRCh38
NC_000002.11:g.233406002T>G , CM000664.1:g.233406002T>G GRCh37
NC_000002.10:g.233114246T>G NCBI36
NG_012954.1:g.6566T>G
NG_012954.2:g.6601T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.351-82T>G MANE Select ENSP00000498757.1:n.351-82T>G
ENST00000389492.3:c.350+581T>G ENSP00000374143.3:n.350+581T>G
ENST00000389494.7:c.351-82T>G ENSP00000374145.3:n.351-82T>G
ENST00000485094.1:n.372-82T>G
NM_005199.4:c.351-82T>G NP_005190.4:n.351-82T>G
NM_005199.5:c.351-82T>G MANE Select NP_005190.4:n.351-82T>G
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