Canonical Allele Identifier: CA309124279
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs996039546
gnomAD v2: 19-47507374-T-C
gnomAD v3: 19-47004117-T-C
gnomAD v4: 19-47004117-T-C
MyVariant Identifiers: chr19:g.47507374T>C (hg19) chr19:g.47004117T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004117T>C , CM000681.2:g.47004117T>C GRCh38
NC_000019.9:g.47507374T>C , CM000681.1:g.47507374T>C GRCh37
NC_000019.8:g.52199214T>C NCBI36
NG_047014.1:g.90551T>C
NG_047014.2:g.148121T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7929T>C ENSP00000385720.2:n.7929T>C
ENST00000672722.1:c.*3429T>C MANE Select ENSP00000500409.1:n.*3429T>C
ENST00000404338.7:c.7929T>C ENSP00000385720.2:n.7929T>C
ENST00000614079.1:c.7506T>C ENSP00000483730.1:n.7506T>C
NM_004491.4:c.7929T>C NP_004482.4:n.7929T>C
NM_004491.5:c.*3429T>C MANE Select NP_004482.4:n.*3429T>C
Search 100 bp 5'
Search 100 bp 3'