Canonical Allele Identifier: CA633401867
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs1568493936
gnomAD v2: 19-47507208-A-AC
gnomAD v3: 19-47003951-A-AC
gnomAD v4: 19-47003951-A-AC
MyVariant Identifiers: chr19:g.47507208_47507209insC (hg19) chr19:g.47003951_47003952insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003951_47003952insC , CM000681.2:g.47003951_47003952insC GRCh38
NC_000019.9:g.47507208_47507209insC , CM000681.1:g.47507208_47507209insC GRCh37
NC_000019.8:g.52199048_52199049insC NCBI36
NG_047014.1:g.90385_90386insC
NG_047014.2:g.147955_147956insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7763_7764insC ENSP00000385720.2:n.7763_7764insC
ENST00000672722.1:c.*3263_*3264insC MANE Select ENSP00000500409.1:n.*3263_*3264insC
ENST00000404338.7:c.7763_7764insC ENSP00000385720.2:n.7763_7764insC
ENST00000614079.1:c.7340_7341insC ENSP00000483730.1:n.7340_7341insC
NM_004491.4:c.7763_7764insC NP_004482.4:n.7763_7764insC
NM_004491.5:c.*3263_*3264insC MANE Select NP_004482.4:n.*3263_*3264insC
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