Canonical Allele Identifier: CA393624743
Gene: ARNT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.80883935T>A (hg19) chr15:g.80591594T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80591594T>A , CM000677.2:g.80591594T>A GRCh38
NC_000015.9:g.80883935T>A , CM000677.1:g.80883935T>A GRCh37
NC_000015.8:g.78670990T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303329.9:c.1945T>A MANE Select ENSP00000307479.4:p.Phe649Ile
ENST00000303329.8:c.1945T>A ENSP00000307479.4:p.Phe649Ile
ENST00000527771.5:c.1912T>A ENSP00000453792.1:p.Phe638Ile
ENST00000533983.5:c.1912T>A ENSP00000453651.1:p.Phe638Ile
ENST00000610490.4:c.*243T>A ENSP00000483762.1:n.*243T>A
ENST00000622346.4:c.1945T>A ENSP00000479393.1:p.Phe649Ile
NM_014862.3:c.1945T>A NP_055677.3:p.Phe649Ile
NM_014862.4:c.1945T>A MANE Select NP_055677.3:p.Phe649Ile
Search 100 bp 5'
Search 100 bp 3'