Canonical Allele Identifier: CA309123880

Gene: ARHGAP35

Linked Data

• dbSNP Id: rs527630955
• MyVariant Identifiers: chr19:g.47507080C>T (hg19) ; chr19:g.47003823C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.47003823C>T , CM000681.2:g.47003823C>T	GRCh38
NC_000019.9:g.47507080C>T , CM000681.1:g.47507080C>T	GRCh37
NC_000019.8:g.52198920C>T	NCBI36
NG_047014.1:g.90257C>T
NG_047014.2:g.147827C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404338.8:c.7635C>T	ENSP00000385720.2:n.7635C>T
ENST00000672722.1:c.*3135C>T MANE Select	ENSP00000500409.1:n.*3135C>T
ENST00000404338.7:c.7635C>T	ENSP00000385720.2:n.7635C>T
ENST00000614079.1:c.7212C>T	ENSP00000483730.1:n.7212C>T
NM_004491.4:c.7635C>T	NP_004482.4:n.7635C>T
NM_004491.5:c.*3135C>T MANE Select	NP_004482.4:n.*3135C>T