Canonical Allele Identifier: CA2190489528
Gene: ARNT2 HGNC NCBI

Linked Data

dbSNP Id: rs1893279908
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.80591542A>G , CM000677.2:g.80591542A>G GRCh38
NC_000015.9:g.80883883A>G , CM000677.1:g.80883883A>G GRCh37
NC_000015.8:g.78670938A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303329.9:c.1919-26A>G MANE Select ENSP00000307479.4:n.1919-26A>G
ENST00000303329.8:c.1919-26A>G ENSP00000307479.4:n.1919-26A>G
ENST00000527771.5:c.1886-26A>G ENSP00000453792.1:n.1886-26A>G
ENST00000533983.5:c.1886-26A>G ENSP00000453651.1:n.1886-26A>G
ENST00000610490.4:c.*217-26A>G ENSP00000483762.1:n.*217-26A>G
ENST00000622346.4:c.1919-26A>G ENSP00000479393.1:n.1919-26A>G
NM_014862.3:c.1919-26A>G NP_055677.3:n.1919-26A>G
NM_014862.4:c.1919-26A>G MANE Select NP_055677.3:n.1919-26A>G
Search 100 bp 5'
Search 100 bp 3'