Canonical Allele Identifier: CA633401866
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs57048215
gnomAD v2: 19-47507207-A-AC
gnomAD v3: 19-47003950-A-AC
gnomAD v4: 19-47003950-A-AC
MyVariant Identifiers: chr19:g.47507207_47507208insC (hg19) chr19:g.47003950_47003951insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003950_47003951insC , CM000681.2:g.47003950_47003951insC GRCh38
NC_000019.9:g.47507207_47507208insC , CM000681.1:g.47507207_47507208insC GRCh37
NC_000019.8:g.52199047_52199048insC NCBI36
NG_047014.1:g.90384_90385insC
NG_047014.2:g.147954_147955insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7762_7763insC ENSP00000385720.2:n.7762_7763insC
ENST00000672722.1:c.*3262_*3263insC MANE Select ENSP00000500409.1:n.*3262_*3263insC
ENST00000404338.7:c.7762_7763insC ENSP00000385720.2:n.7762_7763insC
ENST00000614079.1:c.7339_7340insC ENSP00000483730.1:n.7339_7340insC
NM_004491.4:c.7762_7763insC NP_004482.4:n.7762_7763insC
NM_004491.5:c.*3262_*3263insC MANE Select NP_004482.4:n.*3262_*3263insC
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