Canonical Allele Identifier: CA7751082
Gene: ARRDC4 HGNC NCBI

Linked Data

dbSNP Id: rs200944490
ExAC: 15:98504164 G / C
gnomAD v2: 15-98504164-G-C
gnomAD v3: 15-97960934-G-C
gnomAD v4: 15-97960934-G-C
MyVariant Identifiers: chr15:g.98504164G>C (hg19) chr15:g.97960934G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.97960934G>C , CM000677.2:g.97960934G>C GRCh38
NC_000015.9:g.98504164G>C , CM000677.1:g.98504164G>C GRCh37
NC_000015.8:g.96305168G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000268042.7:c.73G>C MANE Select ENSP00000268042.6:p.Glu25Gln
ENST00000268042.6:c.73G>C ENSP00000268042.6:p.Glu25Gln
NM_183376.2:c.73G>C NP_899232.2:p.Glu25Gln
NM_183376.3:c.73G>C MANE Select NP_899232.2:p.Glu25Gln
Search 100 bp 5'
Search 100 bp 3'