Canonical Allele Identifier: CA633401858
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs1197454229
gnomAD v2: 19-47507146-C-A
gnomAD v4: 19-47003889-C-A
MyVariant Identifiers: chr19:g.47507146C>A (hg19) chr19:g.47003889C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003889C>A , CM000681.2:g.47003889C>A GRCh38
NC_000019.9:g.47507146C>A , CM000681.1:g.47507146C>A GRCh37
NC_000019.8:g.52198986C>A NCBI36
NG_047014.1:g.90323C>A
NG_047014.2:g.147893C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7701C>A ENSP00000385720.2:n.7701C>A
ENST00000672722.1:c.*3201C>A MANE Select ENSP00000500409.1:n.*3201C>A
ENST00000404338.7:c.7701C>A ENSP00000385720.2:n.7701C>A
ENST00000614079.1:c.7278C>A ENSP00000483730.1:n.7278C>A
NM_004491.4:c.7701C>A NP_004482.4:n.7701C>A
NM_004491.5:c.*3201C>A MANE Select NP_004482.4:n.*3201C>A
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