Canonical Allele Identifier: CA431810958
Gene: CHRNG HGNC NCBI

Linked Data

gnomAD v4: 2-232542994-C-T
MyVariant Identifiers: chr2:g.233407704C>T (hg19)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000651502.1:c.717C>T MANE Select ENSP00000498757.1:p.Arg239=
ENST00000389492.3:c.561C>T ENSP00000374143.3:p.Arg187=
ENST00000389494.7:c.717C>T ENSP00000374145.3:p.Arg239=
NM_005199.4:c.717C>T NP_005190.4:p.Arg239=
NM_005199.5:c.717C>T MANE Select NP_005190.4:p.Arg239=
Search 100 bp 5'
Search 100 bp 3'