Canonical Allele Identifier: CA393624731
Gene: ARNT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.80883929G>C (hg19) chr15:g.80591588G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80591588G>C , CM000677.2:g.80591588G>C GRCh38
NC_000015.9:g.80883929G>C , CM000677.1:g.80883929G>C GRCh37
NC_000015.8:g.78670984G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303329.9:c.1939G>C MANE Select ENSP00000307479.4:p.Gly647Arg
ENST00000303329.8:c.1939G>C ENSP00000307479.4:p.Gly647Arg
ENST00000527771.5:c.1906G>C ENSP00000453792.1:p.Gly636Arg
ENST00000533983.5:c.1906G>C ENSP00000453651.1:p.Gly636Arg
ENST00000610490.4:c.*237G>C ENSP00000483762.1:n.*237G>C
ENST00000622346.4:c.1939G>C ENSP00000479393.1:p.Gly647Arg
NM_014862.3:c.1939G>C NP_055677.3:p.Gly647Arg
NM_014862.4:c.1939G>C MANE Select NP_055677.3:p.Gly647Arg
Search 100 bp 5'
Search 100 bp 3'