Canonical Allele Identifier: CA309123997
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs145676771
gnomAD v2: 19-47507171-ACACG-A
gnomAD v3: 19-47003914-ACACG-A
gnomAD v4: 19-47003914-ACACG-A
MyVariant Identifiers: chr19:g.47507172_47507175del (hg19) chr19:g.47003915_47003918del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003918_47003921del , CM000681.2:g.47003918_47003921del GRCh38
NC_000019.9:g.47507175_47507178del , CM000681.1:g.47507175_47507178del GRCh37
NC_000019.8:g.52199015_52199018del NCBI36
NG_047014.1:g.90352_90355del
NG_047014.2:g.147922_147925del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7730_7733del ENSP00000385720.2:n.7730_7733del
ENST00000672722.1:c.*3230_*3233del MANE Select ENSP00000500409.1:n.*3230_*3233del
ENST00000404338.7:c.7730_7733del ENSP00000385720.2:n.7730_7733del
ENST00000614079.1:c.7307_7310del ENSP00000483730.1:n.7307_7310del
NM_004491.4:c.7730_7733del NP_004482.4:n.7730_7733del
NM_004491.5:c.*3230_*3233del MANE Select NP_004482.4:n.*3230_*3233del
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