Canonical Allele Identifier: CA309124431
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs576056213
gnomAD v3: 19-47004282-C-T
gnomAD v4: 19-47004282-C-T
MyVariant Identifiers: chr19:g.47507539C>T (hg19) chr19:g.47004282C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004282C>T , CM000681.2:g.47004282C>T GRCh38
NC_000019.9:g.47507539C>T , CM000681.1:g.47507539C>T GRCh37
NC_000019.8:g.52199379C>T NCBI36
NG_047014.1:g.90716C>T
NG_047014.2:g.148286C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.8094C>T ENSP00000385720.2:n.8094C>T
ENST00000672722.1:c.*3594C>T MANE Select ENSP00000500409.1:n.*3594C>T
ENST00000404338.7:c.8094C>T ENSP00000385720.2:n.8094C>T
ENST00000614079.1:c.7671C>T ENSP00000483730.1:n.7671C>T
NM_004491.4:c.8094C>T NP_004482.4:n.8094C>T
NM_004491.5:c.*3594C>T MANE Select NP_004482.4:n.*3594C>T
Search 100 bp 5'
Search 100 bp 3'