Canonical Allele Identifier: CA309124151
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs984333043
gnomAD v2: 19-47507177-A-ACG
gnomAD v3: 19-47003920-A-ACG
gnomAD v4: 19-47003920-A-ACG
MyVariant Identifiers: chr19:g.47507177_47507178insCG (hg19) chr19:g.47003920_47003921insCG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003921_47003922insGC , CM000681.2:g.47003921_47003922insGC GRCh38
NC_000019.9:g.47507178_47507179insGC , CM000681.1:g.47507178_47507179insGC GRCh37
NC_000019.8:g.52199018_52199019insGC NCBI36
NG_047014.1:g.90355_90356insGC
NG_047014.2:g.147925_147926insGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7733_7734insGC ENSP00000385720.2:n.7733_7734insGC
ENST00000672722.1:c.*3233_*3234insGC MANE Select ENSP00000500409.1:n.*3233_*3234insGC
ENST00000404338.7:c.7733_7734insGC ENSP00000385720.2:n.7733_7734insGC
ENST00000614079.1:c.7310_7311insGC ENSP00000483730.1:n.7310_7311insGC
NM_004491.4:c.7733_7734insGC NP_004482.4:n.7733_7734insGC
NM_004491.5:c.*3233_*3234insGC MANE Select NP_004482.4:n.*3233_*3234insGC
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