Canonical Allele Identifier: CA492461990
Gene: ARRDC4 HGNC NCBI

Linked Data

gnomAD v4: 15-97960900-C-A
MyVariant Identifiers: chr15:g.98504130C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.97960900C>A , CM000677.2:g.97960900C>A GRCh38
NC_000015.9:g.98504130C>A , CM000677.1:g.98504130C>A GRCh37
NC_000015.8:g.96305134C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000268042.7:c.39C>A MANE Select ENSP00000268042.6:p.Ala13=
ENST00000268042.6:c.39C>A ENSP00000268042.6:p.Ala13=
NM_183376.2:c.39C>A NP_899232.2:p.Ala13=
NM_183376.3:c.39C>A MANE Select NP_899232.2:p.Ala13=
Search 100 bp 5'
Search 100 bp 3'