Canonical Allele Identifier: CA2168644
Gene: CHRNG HGNC NCBI

Linked Data

dbSNP Id: rs755562229
ExAC: 2:233406091 G / C
gnomAD v2: 2-233406091-G-C
gnomAD v3: 2-232541381-G-C
gnomAD v4: 2-232541381-G-C
MyVariant Identifiers: chr2:g.233406091G>C (hg19) chr2:g.232541381G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232541381G>C , CM000664.2:g.232541381G>C GRCh38
NC_000002.11:g.233406091G>C , CM000664.1:g.233406091G>C GRCh37
NC_000002.10:g.233114335G>C NCBI36
NG_012954.1:g.6655G>C
NG_012954.2:g.6690G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.358G>C MANE Select ENSP00000498757.1:p.Gly120Arg
ENST00000389492.3:c.350+670G>C ENSP00000374143.3:n.350+670G>C
ENST00000389494.7:c.358G>C ENSP00000374145.3:p.Gly120Arg
ENST00000485094.1:n.379G>C
NM_005199.4:c.358G>C NP_005190.4:p.Gly120Arg
NM_005199.5:c.358G>C MANE Select NP_005190.4:p.Gly120Arg
Search 100 bp 5'
Search 100 bp 3'