Canonical Allele Identifier: CA309123912
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs373579387
gnomAD v2: 19-47507122-AG-A
gnomAD v3: 19-47003865-AG-A
gnomAD v4: 19-47003865-AG-A
MyVariant Identifiers: chr19:g.47507123del (hg19) chr19:g.47003866del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003866del , CM000681.2:g.47003866del GRCh38
NC_000019.9:g.47507123del , CM000681.1:g.47507123del GRCh37
NC_000019.8:g.52198963del NCBI36
NG_047014.1:g.90300del
NG_047014.2:g.147870del

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7678del ENSP00000385720.2:n.7678del
ENST00000672722.1:c.*3178del MANE Select ENSP00000500409.1:n.*3178del
ENST00000404338.7:c.7678del ENSP00000385720.2:n.7678del
ENST00000614079.1:c.7255del ENSP00000483730.1:n.7255del
NM_004491.4:c.7678del NP_004482.4:n.7678del
NM_004491.5:c.*3178del MANE Select NP_004482.4:n.*3178del
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Search 100 bp 3'