Canonical Allele Identifier: CA351011989
Gene: CHRNG HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.233407703G>C (hg19) chr2:g.232542993G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232542993G>C , CM000664.2:g.232542993G>C GRCh38
NC_000002.11:g.233407703G>C , CM000664.1:g.233407703G>C GRCh37
NC_000002.10:g.233115947G>C NCBI36
NG_012954.1:g.8267G>C
NG_012954.2:g.8302G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000651502.1:c.716G>C MANE Select ENSP00000498757.1:p.Arg239Pro
ENST00000389492.3:c.560G>C ENSP00000374143.3:p.Arg187Pro
ENST00000389494.7:c.716G>C ENSP00000374145.3:p.Arg239Pro
NM_005199.4:c.716G>C NP_005190.4:p.Arg239Pro
NM_005199.5:c.716G>C MANE Select NP_005190.4:p.Arg239Pro
Search 100 bp 5'
Search 100 bp 3'