Canonical Allele Identifier: CA393660278
Gene: ARRDC4 HGNC NCBI

Linked Data

dbSNP Id: rs1459203586
gnomAD v2: 15-98504092-A-G
gnomAD v4: 15-97960862-A-G
MyVariant Identifiers: chr15:g.98504092A>G (hg19) chr15:g.97960862A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.97960862A>G , CM000677.2:g.97960862A>G GRCh38
NC_000015.9:g.98504092A>G , CM000677.1:g.98504092A>G GRCh37
NC_000015.8:g.96305096A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000268042.7:c.1A>G MANE Select ENSP00000268042.6:p.Met1Val
ENST00000268042.6:c.1A>G ENSP00000268042.6:p.Met1Val
NM_183376.2:c.1A>G NP_899232.2:p.Met1Val
NM_183376.3:c.1A>G MANE Select NP_899232.2:p.Met1Val
Search 100 bp 5'
Search 100 bp 3'