Canonical Allele Identifier: CA633401864
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs1273017040
gnomAD v2: 19-47507179-A-ACG
gnomAD v3: 19-47003922-A-ACG
gnomAD v4: 19-47003922-A-ACG
MyVariant Identifiers: chr19:g.47507179_47507180insCG (hg19) chr19:g.47003922_47003923insCG (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003923_47003924insGC , CM000681.2:g.47003923_47003924insGC GRCh38
NC_000019.9:g.47507180_47507181insGC , CM000681.1:g.47507180_47507181insGC GRCh37
NC_000019.8:g.52199020_52199021insGC NCBI36
NG_047014.1:g.90357_90358insGC
NG_047014.2:g.147927_147928insGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7735_7736insGC ENSP00000385720.2:n.7735_7736insGC
ENST00000672722.1:c.*3235_*3236insGC MANE Select ENSP00000500409.1:n.*3235_*3236insGC
ENST00000404338.7:c.7735_7736insGC ENSP00000385720.2:n.7735_7736insGC
ENST00000614079.1:c.7312_7313insGC ENSP00000483730.1:n.7312_7313insGC
NM_004491.4:c.7735_7736insGC NP_004482.4:n.7735_7736insGC
NM_004491.5:c.*3235_*3236insGC MANE Select NP_004482.4:n.*3235_*3236insGC
Search 100 bp 5'
Search 100 bp 3'