Canonical Allele Identifier: CA2586003878
Gene: ARHGAP35 HGNC NCBI

Linked Data

gnomAD v4: 19-47003982-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003982G>T , CM000681.2:g.47003982G>T GRCh38
NC_000019.9:g.47507239G>T , CM000681.1:g.47507239G>T GRCh37
NC_000019.8:g.52199079G>T NCBI36
NG_047014.1:g.90416G>T
NG_047014.2:g.147986G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7794G>T ENSP00000385720.2:n.7794G>T
ENST00000672722.1:c.*3294G>T MANE Select ENSP00000500409.1:n.*3294G>T
ENST00000404338.7:c.7794G>T ENSP00000385720.2:n.7794G>T
ENST00000614079.1:c.7371G>T ENSP00000483730.1:n.7371G>T
NM_004491.4:c.7794G>T NP_004482.4:n.7794G>T
NM_004491.5:c.*3294G>T MANE Select NP_004482.4:n.*3294G>T
Search 100 bp 5'
Search 100 bp 3'