Canonical Allele Identifier: CA435411843

Gene: ARHGAP31

Linked Data

• dbSNP Id: rs2080746941
• MyVariant Identifiers: chr3:g.119133134C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414287C>T , CM000665.2:g.119414287C>T	GRCh38
NC_000003.11:g.119133134C>T , CM000665.1:g.119133134C>T	GRCh37
NC_000003.10:g.120615824C>T	NCBI36
NG_007665.2:g.124915C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2358C>T MANE Select	ENSP00000264245.4:p.Pro786=
ENST00000264245.8:c.2358C>T	ENSP00000264245.4:p.Pro786=
NM_020754.3:c.2358C>T	NP_065805.2:p.Pro786=
XM_005247671.3:c.2265C>T	XP_005247728.1:p.Pro755=
XM_006713714.2:c.2298C>T	XP_006713777.1:p.Pro766=
XM_006713714.3:c.2298C>T	XP_006713777.1:p.Pro766=
XM_017006955.1:c.1866C>T	XP_016862444.1:p.Pro622=
NM_020754.4:c.2358C>T MANE Select	NP_065805.2:p.Pro786=