Canonical Allele Identifier: CA996445462
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs2056764778
gnomAD v3: 19-47004320-G-A
gnomAD v4: 19-47004320-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004320G>A , CM000681.2:g.47004320G>A GRCh38
NC_000019.9:g.47507577G>A , CM000681.1:g.47507577G>A GRCh37
NC_000019.8:g.52199417G>A NCBI36
NG_047014.1:g.90754G>A
NG_047014.2:g.148324G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.8132G>A ENSP00000385720.2:n.8132G>A
ENST00000672722.1:c.*3632G>A MANE Select ENSP00000500409.1:n.*3632G>A
ENST00000404338.7:c.8132G>A ENSP00000385720.2:n.8132G>A
NM_004491.4:c.8132G>A NP_004482.4:n.8132G>A
NM_004491.5:c.*3632G>A MANE Select NP_004482.4:n.*3632G>A
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