Canonical Allele Identifier: CA996445468
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs2056765058
gnomAD v3: 19-47004349-G-T
gnomAD v4: 19-47004349-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004349G>T , CM000681.2:g.47004349G>T GRCh38
NC_000019.9:g.47507606G>T , CM000681.1:g.47507606G>T GRCh37
NC_000019.8:g.52199446G>T NCBI36
NG_047014.1:g.90783G>T
NG_047014.2:g.148353G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.8161G>T ENSP00000385720.2:n.8161G>T
ENST00000672722.1:c.*3661G>T MANE Select ENSP00000500409.1:n.*3661G>T
ENST00000404338.7:c.8161G>T ENSP00000385720.2:n.8161G>T
NM_004491.4:c.8161G>T NP_004482.4:n.8161G>T
NM_004491.5:c.*3661G>T MANE Select NP_004482.4:n.*3661G>T
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