Canonical Allele Identifier: CA633401862
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs777306146
gnomAD v2: 19-47507173-A-ACG
gnomAD v3: 19-47003916-A-ACG
gnomAD v4: 19-47003916-A-ACG
MyVariant Identifiers: chr19:g.47507175_47507176insCG (hg19) chr19:g.47507173_47507174insCG (hg19) chr19:g.47003918_47003919insCG (hg38) chr19:g.47003916_47003917insCG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003918_47003919dup , CM000681.2:g.47003918_47003919dup GRCh38
NC_000019.9:g.47507175_47507176dup , CM000681.1:g.47507175_47507176dup GRCh37
NC_000019.8:g.52199015_52199016dup NCBI36
NG_047014.1:g.90352_90353dup
NG_047014.2:g.147922_147923dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7730_7731dup ENSP00000385720.2:n.7730_7731dup
ENST00000672722.1:c.*3230_*3231dup MANE Select ENSP00000500409.1:n.*3230_*3231dup
ENST00000404338.7:c.7730_7731dup ENSP00000385720.2:n.7730_7731dup
ENST00000614079.1:c.7307_7308dup ENSP00000483730.1:n.7307_7308dup
NM_004491.4:c.7730_7731dup NP_004482.4:n.7730_7731dup
NM_004491.5:c.*3230_*3231dup MANE Select NP_004482.4:n.*3230_*3231dup
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Search 100 bp 3'