Canonical Allele Identifier: CA882866696
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs1343340912
gnomAD v3: 19-47004005-C-T
gnomAD v4: 19-47004005-C-T
MyVariant Identifiers: chr19:g.47507262C>T (hg19) chr19:g.47004005C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004005C>T , CM000681.2:g.47004005C>T GRCh38
NC_000019.9:g.47507262C>T , CM000681.1:g.47507262C>T GRCh37
NC_000019.8:g.52199102C>T NCBI36
NG_047014.1:g.90439C>T
NG_047014.2:g.148009C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7817C>T ENSP00000385720.2:n.7817C>T
ENST00000672722.1:c.*3317C>T MANE Select ENSP00000500409.1:n.*3317C>T
ENST00000404338.7:c.7817C>T ENSP00000385720.2:n.7817C>T
ENST00000614079.1:c.7394C>T ENSP00000483730.1:n.7394C>T
NM_004491.4:c.7817C>T NP_004482.4:n.7817C>T
NM_004491.5:c.*3317C>T MANE Select NP_004482.4:n.*3317C>T
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