Canonical Allele Identifier: CA2586003718
Gene: ARHGAP35 HGNC NCBI

Linked Data

gnomAD v4: 19-47003888-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003888C>A , CM000681.2:g.47003888C>A GRCh38
NC_000019.9:g.47507145C>A , CM000681.1:g.47507145C>A GRCh37
NC_000019.8:g.52198985C>A NCBI36
NG_047014.1:g.90322C>A
NG_047014.2:g.147892C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7700C>A ENSP00000385720.2:n.7700C>A
ENST00000672722.1:c.*3200C>A MANE Select ENSP00000500409.1:n.*3200C>A
ENST00000404338.7:c.7700C>A ENSP00000385720.2:n.7700C>A
ENST00000614079.1:c.7277C>A ENSP00000483730.1:n.7277C>A
NM_004491.4:c.7700C>A NP_004482.4:n.7700C>A
NM_004491.5:c.*3200C>A MANE Select NP_004482.4:n.*3200C>A
Search 100 bp 5'
Search 100 bp 3'