Canonical Allele Identifier: CA2586004307
Gene: ARHGAP35 HGNC NCBI

Linked Data

gnomAD v4: 19-47004387-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004387C>A , CM000681.2:g.47004387C>A GRCh38
NC_000019.9:g.47507644C>A , CM000681.1:g.47507644C>A GRCh37
NC_000019.8:g.52199484C>A NCBI36
NG_047014.1:g.90821C>A
NG_047014.2:g.148391C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.8199C>A ENSP00000385720.2:n.8199C>A
ENST00000672722.1:c.*3699C>A MANE Select ENSP00000500409.1:n.*3699C>A
ENST00000404338.7:c.8199C>A ENSP00000385720.2:n.8199C>A
NM_004491.4:c.8199C>A NP_004482.4:n.8199C>A
NM_004491.5:c.*3699C>A MANE Select NP_004482.4:n.*3699C>A
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