Canonical Allele Identifier: CA882866766
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs1409782535
MyVariant Identifiers: chr19:g.47507339G>A (hg19) chr19:g.47004082G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004082G>A , CM000681.2:g.47004082G>A GRCh38
NC_000019.9:g.47507339G>A , CM000681.1:g.47507339G>A GRCh37
NC_000019.8:g.52199179G>A NCBI36
NG_047014.1:g.90516G>A
NG_047014.2:g.148086G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000404338.8:c.7894G>A ENSP00000385720.2:n.7894G>A
ENST00000672722.1:c.*3394G>A MANE Select ENSP00000500409.1:n.*3394G>A
ENST00000404338.7:c.7894G>A ENSP00000385720.2:n.7894G>A
ENST00000614079.1:c.7471G>A ENSP00000483730.1:n.7471G>A
NM_004491.4:c.7894G>A NP_004482.4:n.7894G>A
NM_004491.5:c.*3394G>A MANE Select NP_004482.4:n.*3394G>A
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