Canonical Allele Identifier: CA431810542
Gene: CHRNG HGNC NCBI

Linked Data

COSMIC: COSM5441338
MyVariant Identifiers: chr2:g.233406234C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232541524C>T , CM000664.2:g.232541524C>T GRCh38
NC_000002.11:g.233406234C>T , CM000664.1:g.233406234C>T GRCh37
NC_000002.10:g.233114478C>T NCBI36
NG_012954.1:g.6798C>T
NG_012954.2:g.6833C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.501C>T MANE Select ENSP00000498757.1:p.Ile167=
ENST00000389492.3:c.350+813C>T ENSP00000374143.3:n.350+813C>T
ENST00000389494.7:c.501C>T ENSP00000374145.3:p.Ile167=
ENST00000485094.1:n.522C>T
NM_005199.4:c.501C>T NP_005190.4:p.Ile167=
NM_005199.5:c.501C>T MANE Select NP_005190.4:p.Ile167=
Search 100 bp 5'
Search 100 bp 3'