Canonical Allele Identifier: CA2586003704
Gene: ARHGAP35 HGNC NCBI

Linked Data

gnomAD v4: 19-47003883-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003883A>G , CM000681.2:g.47003883A>G GRCh38
NC_000019.9:g.47507140A>G , CM000681.1:g.47507140A>G GRCh37
NC_000019.8:g.52198980A>G NCBI36
NG_047014.1:g.90317A>G
NG_047014.2:g.147887A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7695A>G ENSP00000385720.2:n.7695A>G
ENST00000672722.1:c.*3195A>G MANE Select ENSP00000500409.1:n.*3195A>G
ENST00000404338.7:c.7695A>G ENSP00000385720.2:n.7695A>G
ENST00000614079.1:c.7272A>G ENSP00000483730.1:n.7272A>G
NM_004491.4:c.7695A>G NP_004482.4:n.7695A>G
NM_004491.5:c.*3195A>G MANE Select NP_004482.4:n.*3195A>G
Search 100 bp 5'
Search 100 bp 3'