Canonical Allele Identifier: CA309123906
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs1013566393
gnomAD v2: 19-47507121-A-G
gnomAD v3: 19-47003864-A-G
gnomAD v4: 19-47003864-A-G
MyVariant Identifiers: chr19:g.47507121A>G (hg19) chr19:g.47003864A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003864A>G , CM000681.2:g.47003864A>G GRCh38
NC_000019.9:g.47507121A>G , CM000681.1:g.47507121A>G GRCh37
NC_000019.8:g.52198961A>G NCBI36
NG_047014.1:g.90298A>G
NG_047014.2:g.147868A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7676A>G ENSP00000385720.2:n.7676A>G
ENST00000672722.1:c.*3176A>G MANE Select ENSP00000500409.1:n.*3176A>G
ENST00000404338.7:c.7676A>G ENSP00000385720.2:n.7676A>G
ENST00000614079.1:c.7253A>G ENSP00000483730.1:n.7253A>G
NM_004491.4:c.7676A>G NP_004482.4:n.7676A>G
NM_004491.5:c.*3176A>G MANE Select NP_004482.4:n.*3176A>G
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