Canonical Allele Identifier: CA882866667
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs1377180661
gnomAD v3: 19-47003937-C-CAA
gnomAD v4: 19-47003937-C-CAA
MyVariant Identifiers: chr19:g.47507194_47507195insAA (hg19) chr19:g.47003937_47003938insAA (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003938_47003939insAA , CM000681.2:g.47003938_47003939insAA GRCh38
NC_000019.9:g.47507195_47507196insAA , CM000681.1:g.47507195_47507196insAA GRCh37
NC_000019.8:g.52199035_52199036insAA NCBI36
NG_047014.1:g.90372_90373insAA
NG_047014.2:g.147942_147943insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7750_7751insAA ENSP00000385720.2:n.7750_7751insAA
ENST00000672722.1:c.*3250_*3251insAA MANE Select ENSP00000500409.1:n.*3250_*3251insAA
ENST00000404338.7:c.7750_7751insAA ENSP00000385720.2:n.7750_7751insAA
ENST00000614079.1:c.7327_7328insAA ENSP00000483730.1:n.7327_7328insAA
NM_004491.4:c.7750_7751insAA NP_004482.4:n.7750_7751insAA
NM_004491.5:c.*3250_*3251insAA MANE Select NP_004482.4:n.*3250_*3251insAA
Search 100 bp 5'
Search 100 bp 3'