Canonical Allele Identifier: CA431810381
Gene: CHRNG HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.233406147C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232541437C>A , CM000664.2:g.232541437C>A GRCh38
NC_000002.11:g.233406147C>A , CM000664.1:g.233406147C>A GRCh37
NC_000002.10:g.233114391C>A NCBI36
NG_012954.1:g.6711C>A
NG_012954.2:g.6746C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.414C>A MANE Select ENSP00000498757.1:p.Ile138=
ENST00000389492.3:c.350+726C>A ENSP00000374143.3:n.350+726C>A
ENST00000389494.7:c.414C>A ENSP00000374145.3:p.Ile138=
ENST00000485094.1:n.435C>A
NM_005199.4:c.414C>A NP_005190.4:p.Ile138=
NM_005199.5:c.414C>A MANE Select NP_005190.4:p.Ile138=
Search 100 bp 5'
Search 100 bp 3'