Canonical Allele Identifier: CA309124353
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs927071926
gnomAD v4: 19-47004158-A-C
MyVariant Identifiers: chr19:g.47507415A>C (hg19) chr19:g.47004158A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004158A>C , CM000681.2:g.47004158A>C GRCh38
NC_000019.9:g.47507415A>C , CM000681.1:g.47507415A>C GRCh37
NC_000019.8:g.52199255A>C NCBI36
NG_047014.1:g.90592A>C
NG_047014.2:g.148162A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7970A>C ENSP00000385720.2:n.7970A>C
ENST00000672722.1:c.*3470A>C MANE Select ENSP00000500409.1:n.*3470A>C
ENST00000404338.7:c.7970A>C ENSP00000385720.2:n.7970A>C
ENST00000614079.1:c.7547A>C ENSP00000483730.1:n.7547A>C
NM_004491.4:c.7970A>C NP_004482.4:n.7970A>C
NM_004491.5:c.*3470A>C MANE Select NP_004482.4:n.*3470A>C
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