Canonical Allele Identifier: CA492462014
Gene: ARRDC4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.98504160G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.97960930G>C , CM000677.2:g.97960930G>C GRCh38
NC_000015.9:g.98504160G>C , CM000677.1:g.98504160G>C GRCh37
NC_000015.8:g.96305164G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000268042.7:c.69G>C MANE Select ENSP00000268042.6:p.Val23=
ENST00000268042.6:c.69G>C ENSP00000268042.6:p.Val23=
NM_183376.2:c.69G>C NP_899232.2:p.Val23=
NM_183376.3:c.69G>C MANE Select NP_899232.2:p.Val23=