Canonical Allele Identifier: CA2553993
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs764589379

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414175T>A , CM000665.2:g.119414175T>A GRCh38
NC_000003.11:g.119133022T>A , CM000665.1:g.119133022T>A GRCh37
NC_000003.10:g.120615712T>A NCBI36
NG_007665.2:g.124803T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2246T>A MANE Select ENSP00000264245.4:p.Leu749His
ENST00000264245.8:c.2246T>A ENSP00000264245.4:p.Leu749His
NM_020754.3:c.2246T>A NP_065805.2:p.Leu749His
XM_005247671.3:c.2153T>A XP_005247728.1:p.Leu718His
XM_006713714.2:c.2186T>A XP_006713777.1:p.Leu729His
XM_006713714.3:c.2186T>A XP_006713777.1:p.Leu729His
XM_017006955.1:c.1754T>A XP_016862444.1:p.Leu585His
NM_020754.4:c.2246T>A MANE Select NP_065805.2:p.Leu749His