Canonical Allele Identifier: CA882866833
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs1378624401
gnomAD v4: 19-47004209-G-A
MyVariant Identifiers: chr19:g.47507466G>A (hg19) chr19:g.47004209G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004209G>A , CM000681.2:g.47004209G>A GRCh38
NC_000019.9:g.47507466G>A , CM000681.1:g.47507466G>A GRCh37
NC_000019.8:g.52199306G>A NCBI36
NG_047014.1:g.90643G>A
NG_047014.2:g.148213G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.8021G>A ENSP00000385720.2:n.8021G>A
ENST00000672722.1:c.*3521G>A MANE Select ENSP00000500409.1:n.*3521G>A
ENST00000404338.7:c.8021G>A ENSP00000385720.2:n.8021G>A
ENST00000614079.1:c.7598G>A ENSP00000483730.1:n.7598G>A
NM_004491.4:c.8021G>A NP_004482.4:n.8021G>A
NM_004491.5:c.*3521G>A MANE Select NP_004482.4:n.*3521G>A
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