Canonical Allele Identifier: CA2339183763

Gene: ARHGAP35

Linked Data

• dbSNP Id: rs2056765232

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47004375C>T , CM000681.2:g.47004375C>T	GRCh38
NC_000019.9:g.47507632C>T , CM000681.1:g.47507632C>T	GRCh37
NC_000019.8:g.52199472C>T	NCBI36
NG_047014.1:g.90809C>T
NG_047014.2:g.148379C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404338.8:c.8187C>T	ENSP00000385720.2:n.8187C>T
ENST00000672722.1:c.*3687C>T MANE Select	ENSP00000500409.1:n.*3687C>T
ENST00000404338.7:c.8187C>T	ENSP00000385720.2:n.8187C>T
NM_004491.4:c.8187C>T	NP_004482.4:n.8187C>T
NM_004491.5:c.*3687C>T MANE Select	NP_004482.4:n.*3687C>T