Canonical Allele Identifier: CA351012069
Gene: CHRNG HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.233407715T>A (hg19) chr2:g.232543005T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232543005T>A , CM000664.2:g.232543005T>A GRCh38
NC_000002.11:g.233407715T>A , CM000664.1:g.233407715T>A GRCh37
NC_000002.10:g.233115959T>A NCBI36
NG_012954.1:g.8279T>A
NG_012954.2:g.8314T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000651502.1:c.728T>A MANE Select ENSP00000498757.1:p.Phe243Tyr
ENST00000389492.3:c.572T>A ENSP00000374143.3:p.Phe191Tyr
ENST00000389494.7:c.728T>A ENSP00000374145.3:p.Phe243Tyr
NM_005199.4:c.728T>A NP_005190.4:p.Phe243Tyr
NM_005199.5:c.728T>A MANE Select NP_005190.4:p.Phe243Tyr
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