Canonical Allele Identifier: CA2701787596
Gene: CHRNG HGNC NCBI

Linked Data

dbSNP Id: rs2106220809
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232541635C>A , CM000664.2:g.232541635C>A GRCh38
NC_000002.11:g.233406345C>A , CM000664.1:g.233406345C>A GRCh37
NC_000002.10:g.233114589C>A NCBI36
NG_012954.1:g.6909C>A
NG_012954.2:g.6944C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.506+106C>A MANE Select ENSP00000498757.1:n.506+106C>A
ENST00000389492.3:c.351-788C>A ENSP00000374143.3:n.351-788C>A
ENST00000389494.7:c.506+106C>A ENSP00000374145.3:n.506+106C>A
ENST00000485094.1:n.633C>A
NM_005199.4:c.506+106C>A NP_005190.4:n.506+106C>A
NM_005199.5:c.506+106C>A MANE Select NP_005190.4:n.506+106C>A
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