Canonical Allele Identifier: CA351006794
Gene: CHRNG HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.233404504T>A (hg19) chr2:g.232539794T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232539794T>A , CM000664.2:g.232539794T>A GRCh38
NC_000002.11:g.233404504T>A , CM000664.1:g.233404504T>A GRCh37
NC_000002.10:g.233112748T>A NCBI36
NG_012954.1:g.5068T>A
NG_012954.2:g.5103T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.47T>A MANE Select ENSP00000498757.1:p.Val16Asp
ENST00000389492.3:c.47T>A ENSP00000374143.3:p.Val16Asp
ENST00000389494.7:c.47T>A ENSP00000374145.3:p.Val16Asp
ENST00000485094.1:n.68T>A
NM_005199.4:c.47T>A NP_005190.4:p.Val16Asp
NM_005199.5:c.47T>A MANE Select NP_005190.4:p.Val16Asp
Search 100 bp 5'
Search 100 bp 3'