Canonical Allele Identifier: CA393660559
Gene: ARRDC4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.98504165A>T (hg19) chr15:g.97960935A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.97960935A>T , CM000677.2:g.97960935A>T GRCh38
NC_000015.9:g.98504165A>T , CM000677.1:g.98504165A>T GRCh37
NC_000015.8:g.96305169A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000268042.7:c.74A>T MANE Select ENSP00000268042.6:p.Glu25Val
ENST00000268042.6:c.74A>T ENSP00000268042.6:p.Glu25Val
NM_183376.2:c.74A>T NP_899232.2:p.Glu25Val
NM_183376.3:c.74A>T MANE Select NP_899232.2:p.Glu25Val
Search 100 bp 5'
Search 100 bp 3'