Canonical Allele Identifier: CA275330630
Gene: ARRDC4 HGNC NCBI

Linked Data

dbSNP Id: rs773901599
gnomAD v2: 15-98504152-G-C
gnomAD v3: 15-97960922-G-C
gnomAD v4: 15-97960922-G-C
MyVariant Identifiers: chr15:g.98504152G>C (hg19) chr15:g.97960922G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.97960922G>C , CM000677.2:g.97960922G>C GRCh38
NC_000015.9:g.98504152G>C , CM000677.1:g.98504152G>C GRCh37
NC_000015.8:g.96305156G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000268042.7:c.61G>C MANE Select ENSP00000268042.6:p.Gly21Arg
ENST00000268042.6:c.61G>C ENSP00000268042.6:p.Gly21Arg
NM_183376.2:c.61G>C NP_899232.2:p.Gly21Arg
NM_183376.3:c.61G>C MANE Select NP_899232.2:p.Gly21Arg
Search 100 bp 5'
Search 100 bp 3'