Canonical Allele Identifier: CA2168682
Gene: CHRNG HGNC NCBI

Linked Data

dbSNP Id: rs760199351
ExAC: 2:233406228 C / G
gnomAD v2: 2-233406228-C-G
gnomAD v4: 2-232541518-C-G
MyVariant Identifiers: chr2:g.233406228C>G (hg19) chr2:g.232541518C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232541518C>G , CM000664.2:g.232541518C>G GRCh38
NC_000002.11:g.233406228C>G , CM000664.1:g.233406228C>G GRCh37
NC_000002.10:g.233114472C>G NCBI36
NG_012954.1:g.6792C>G
NG_012954.2:g.6827C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.495C>G MANE Select ENSP00000498757.1:p.Ser165=
ENST00000389492.3:c.350+807C>G ENSP00000374143.3:n.350+807C>G
ENST00000389494.7:c.495C>G ENSP00000374145.3:p.Ser165=
ENST00000485094.1:n.516C>G
NM_005199.4:c.495C>G NP_005190.4:p.Ser165=
NM_005199.5:c.495C>G MANE Select NP_005190.4:p.Ser165=
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