Canonical Allele Identifier: CA492461964
Gene: ARRDC4 HGNC NCBI

Linked Data

dbSNP Id: rs1351114557
gnomAD v2: 15-98504097-C-T
gnomAD v4: 15-97960867-C-T
MyVariant Identifiers: chr15:g.98504097C>T (hg19) chr15:g.97960867C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.97960867C>T , CM000677.2:g.97960867C>T GRCh38
NC_000015.9:g.98504097C>T , CM000677.1:g.98504097C>T GRCh37
NC_000015.8:g.96305101C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000268042.7:c.6C>T MANE Select ENSP00000268042.6:p.Gly2=
ENST00000268042.6:c.6C>T ENSP00000268042.6:p.Gly2=
NM_183376.2:c.6C>T NP_899232.2:p.Gly2=
NM_183376.3:c.6C>T MANE Select NP_899232.2:p.Gly2=
Search 100 bp 5'
Search 100 bp 3'