Canonical Allele Identifier: CA393660357
Gene: ARRDC4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.98504108G>C (hg19) chr15:g.97960878G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.97960878G>C , CM000677.2:g.97960878G>C GRCh38
NC_000015.9:g.98504108G>C , CM000677.1:g.98504108G>C GRCh37
NC_000015.8:g.96305112G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000268042.7:c.17G>C MANE Select ENSP00000268042.6:p.Gly6Ala
ENST00000268042.6:c.17G>C ENSP00000268042.6:p.Gly6Ala
NM_183376.2:c.17G>C NP_899232.2:p.Gly6Ala
NM_183376.3:c.17G>C MANE Select NP_899232.2:p.Gly6Ala
Search 100 bp 5'
Search 100 bp 3'