Canonical Allele Identifier: CA2814602918
Gene: ARHGAP35 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.47004368T>C , CM000681.2:g.47004368T>C GRCh38
NC_000019.9:g.47507625T>C , CM000681.1:g.47507625T>C GRCh37
NC_000019.8:g.52199465T>C NCBI36
NG_047014.1:g.90802T>C
NG_047014.2:g.148372T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000404338.8:c.8180T>C ENSP00000385720.2:n.8180T>C
ENST00000672722.1:c.*3680T>C MANE Select ENSP00000500409.1:n.*3680T>C
ENST00000404338.7:c.8180T>C ENSP00000385720.2:n.8180T>C
NM_004491.4:c.8180T>C NP_004482.4:n.8180T>C
NM_004491.5:c.*3680T>C MANE Select NP_004482.4:n.*3680T>C
Search 100 bp 5'
Search 100 bp 3'