Canonical Allele Identifier: CA2630554042
Gene: ARRDC4 HGNC NCBI

Linked Data

dbSNP Id: rs1899294675
gnomAD v4: 15-97960846-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.97960846A>C , CM000677.2:g.97960846A>C GRCh38
NC_000015.9:g.98504076A>C , CM000677.1:g.98504076A>C GRCh37
NC_000015.8:g.96305080A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000268042.7:c.-16A>C MANE Select ENSP00000268042.6:n.-16A>C
ENST00000268042.6:c.-16A>C ENSP00000268042.6:n.-16A>C
NM_183376.2:c.-16A>C NP_899232.2:n.-16A>C
NM_183376.3:c.-16A>C MANE Select NP_899232.2:n.-16A>C
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