Canonical Allele Identifier: CA882866692
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs1204997486
gnomAD v4: 19-47004003-T-C
MyVariant Identifiers: chr19:g.47507260T>C (hg19) chr19:g.47004003T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004003T>C , CM000681.2:g.47004003T>C GRCh38
NC_000019.9:g.47507260T>C , CM000681.1:g.47507260T>C GRCh37
NC_000019.8:g.52199100T>C NCBI36
NG_047014.1:g.90437T>C
NG_047014.2:g.148007T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7815T>C ENSP00000385720.2:n.7815T>C
ENST00000672722.1:c.*3315T>C MANE Select ENSP00000500409.1:n.*3315T>C
ENST00000404338.7:c.7815T>C ENSP00000385720.2:n.7815T>C
ENST00000614079.1:c.7392T>C ENSP00000483730.1:n.7392T>C
NM_004491.4:c.7815T>C NP_004482.4:n.7815T>C
NM_004491.5:c.*3315T>C MANE Select NP_004482.4:n.*3315T>C
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