Canonical Allele Identifier: CA492462018
Gene: ARRDC4 HGNC NCBI

Linked Data

gnomAD v4: 15-97960936-G-A
MyVariant Identifiers: chr15:g.98504166G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.97960936G>A , CM000677.2:g.97960936G>A GRCh38
NC_000015.9:g.98504166G>A , CM000677.1:g.98504166G>A GRCh37
NC_000015.8:g.96305170G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000268042.7:c.75G>A MANE Select ENSP00000268042.6:p.Glu25=
ENST00000268042.6:c.75G>A ENSP00000268042.6:p.Glu25=
NM_183376.2:c.75G>A NP_899232.2:p.Glu25=
NM_183376.3:c.75G>A MANE Select NP_899232.2:p.Glu25=
Search 100 bp 5'
Search 100 bp 3'