Canonical Allele Identifier: CA492462023
Gene: ARRDC4 HGNC NCBI

Linked Data

dbSNP Id: rs1334691256
gnomAD v4: 15-97960945-C-T
MyVariant Identifiers: chr15:g.98504175C>T (hg19) chr15:g.97960945C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.97960945C>T , CM000677.2:g.97960945C>T GRCh38
NC_000015.9:g.98504175C>T , CM000677.1:g.98504175C>T GRCh37
NC_000015.8:g.96305179C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000268042.7:c.84C>T MANE Select ENSP00000268042.6:p.Arg28=
ENST00000268042.6:c.84C>T ENSP00000268042.6:p.Arg28=
NM_183376.2:c.84C>T NP_899232.2:p.Arg28=
NM_183376.3:c.84C>T MANE Select NP_899232.2:p.Arg28=
Search 100 bp 5'
Search 100 bp 3'