Canonical Allele Identifier: CA2339183414
Gene: ARHGAP35 HGNC NCBI

Linked Data

dbSNP Id: rs2056761343

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47003875C>T , CM000681.2:g.47003875C>T GRCh38
NC_000019.9:g.47507132C>T , CM000681.1:g.47507132C>T GRCh37
NC_000019.8:g.52198972C>T NCBI36
NG_047014.1:g.90309C>T
NG_047014.2:g.147879C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.7687C>T ENSP00000385720.2:n.7687C>T
ENST00000672722.1:c.*3187C>T MANE Select ENSP00000500409.1:n.*3187C>T
ENST00000404338.7:c.7687C>T ENSP00000385720.2:n.7687C>T
ENST00000614079.1:c.7264C>T ENSP00000483730.1:n.7264C>T
NM_004491.4:c.7687C>T NP_004482.4:n.7687C>T
NM_004491.5:c.*3187C>T MANE Select NP_004482.4:n.*3187C>T