Canonical Allele Identifier: CA309124172
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs954596774
gnomAD v3: 19-47003944-A-T
gnomAD v4: 19-47003944-A-T
MyVariant Identifiers: chr19:g.47507201A>T (hg19) chr19:g.47003944A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003944A>T , CM000681.2:g.47003944A>T GRCh38
NC_000019.9:g.47507201A>T , CM000681.1:g.47507201A>T GRCh37
NC_000019.8:g.52199041A>T NCBI36
NG_047014.1:g.90378A>T
NG_047014.2:g.147948A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7756A>T ENSP00000385720.2:n.7756A>T
ENST00000672722.1:c.*3256A>T MANE Select ENSP00000500409.1:n.*3256A>T
ENST00000404338.7:c.7756A>T ENSP00000385720.2:n.7756A>T
ENST00000614079.1:c.7333A>T ENSP00000483730.1:n.7333A>T
NM_004491.4:c.7756A>T NP_004482.4:n.7756A>T
NM_004491.5:c.*3256A>T MANE Select NP_004482.4:n.*3256A>T
Search 100 bp 5'
Search 100 bp 3'