Canonical Allele Identifier: CA351009463
Gene: CHRNG HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.233406236T>A (hg19) chr2:g.232541526T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232541526T>A , CM000664.2:g.232541526T>A GRCh38
NC_000002.11:g.233406236T>A , CM000664.1:g.233406236T>A GRCh37
NC_000002.10:g.233114480T>A NCBI36
NG_012954.1:g.6800T>A
NG_012954.2:g.6835T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.503T>A MANE Select ENSP00000498757.1:p.Phe168Tyr
ENST00000389492.3:c.350+815T>A ENSP00000374143.3:n.350+815T>A
ENST00000389494.7:c.503T>A ENSP00000374145.3:p.Phe168Tyr
ENST00000485094.1:n.524T>A
NM_005199.4:c.503T>A NP_005190.4:p.Phe168Tyr
NM_005199.5:c.503T>A MANE Select NP_005190.4:p.Phe168Tyr
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