Canonical Allele Identifier: CA996445463
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs2056764795
gnomAD v4: 19-47004322-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004322A>G , CM000681.2:g.47004322A>G GRCh38
NC_000019.9:g.47507579A>G , CM000681.1:g.47507579A>G GRCh37
NC_000019.8:g.52199419A>G NCBI36
NG_047014.1:g.90756A>G
NG_047014.2:g.148326A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.8134A>G ENSP00000385720.2:n.8134A>G
ENST00000672722.1:c.*3634A>G MANE Select ENSP00000500409.1:n.*3634A>G
ENST00000404338.7:c.8134A>G ENSP00000385720.2:n.8134A>G
NM_004491.4:c.8134A>G NP_004482.4:n.8134A>G
NM_004491.5:c.*3634A>G MANE Select NP_004482.4:n.*3634A>G
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