Canonical Allele Identifier: CA620299439
Gene: ARRDC4 HGNC NCBI

Linked Data

dbSNP Id: rs1264058725
gnomAD v2: 15-98504079-G-C
gnomAD v4: 15-97960849-G-C
MyVariant Identifiers: chr15:g.98504079G>C (hg19) chr15:g.97960849G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.97960849G>C , CM000677.2:g.97960849G>C GRCh38
NC_000015.9:g.98504079G>C , CM000677.1:g.98504079G>C GRCh37
NC_000015.8:g.96305083G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000268042.7:c.-13G>C MANE Select ENSP00000268042.6:n.-13G>C
ENST00000268042.6:c.-13G>C ENSP00000268042.6:n.-13G>C
NM_183376.2:c.-13G>C NP_899232.2:n.-13G>C
NM_183376.3:c.-13G>C MANE Select NP_899232.2:n.-13G>C
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