Canonical Allele Identifier: CA2553968
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs760835181

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414017A>G , CM000665.2:g.119414017A>G GRCh38
NC_000003.11:g.119132864A>G , CM000665.1:g.119132864A>G GRCh37
NC_000003.10:g.120615554A>G NCBI36
NG_007665.2:g.124645A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2088A>G MANE Select ENSP00000264245.4:p.Ser696=
ENST00000264245.8:c.2088A>G ENSP00000264245.4:p.Ser696=
NM_020754.3:c.2088A>G NP_065805.2:p.Ser696=
XM_005247671.3:c.1995A>G XP_005247728.1:p.Ser665=
XM_006713714.2:c.2028A>G XP_006713777.1:p.Ser676=
XM_006713714.3:c.2028A>G XP_006713777.1:p.Ser676=
XM_017006955.1:c.1596A>G XP_016862444.1:p.Ser532=
NM_020754.4:c.2088A>G MANE Select NP_065805.2:p.Ser696=