Canonical Allele Identifier: CA620299444

Gene: ARRDC4

Linked Data

• dbSNP Id: rs939718188
• gnomAD v2: 15-98504085-C-A
• gnomAD v4: 15-97960855-C-A
• MyVariant Identifiers: chr15:g.98504085C>A (hg19) ; chr15:g.97960855C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.97960855C>A , CM000677.2:g.97960855C>A	GRCh38
NC_000015.9:g.98504085C>A , CM000677.1:g.98504085C>A	GRCh37
NC_000015.8:g.96305089C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268042.7:c.-7C>A MANE Select	ENSP00000268042.6:n.-7C>A
ENST00000268042.6:c.-7C>A	ENSP00000268042.6:n.-7C>A
NM_183376.2:c.-7C>A	NP_899232.2:n.-7C>A
NM_183376.3:c.-7C>A MANE Select	NP_899232.2:n.-7C>A