Canonical Allele Identifier: CA2168776
Gene: CHRNG HGNC NCBI

Linked Data

dbSNP Id: rs764114084
ExAC: 2:233407704 C / G
gnomAD v2: 2-233407704-C-G
MyVariant Identifiers: chr2:g.233407704C>G (hg19) chr2:g.232542994C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232542994C>G , CM000664.2:g.232542994C>G GRCh38
NC_000002.11:g.233407704C>G , CM000664.1:g.233407704C>G GRCh37
NC_000002.10:g.233115948C>G NCBI36
NG_012954.1:g.8268C>G
NG_012954.2:g.8303C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651502.1:c.717C>G MANE Select ENSP00000498757.1:p.Arg239=
ENST00000389492.3:c.561C>G ENSP00000374143.3:p.Arg187=
ENST00000389494.7:c.717C>G ENSP00000374145.3:p.Arg239=
NM_005199.4:c.717C>G NP_005190.4:p.Arg239=
NM_005199.5:c.717C>G MANE Select NP_005190.4:p.Arg239=
Search 100 bp 5'
Search 100 bp 3'