Canonical Allele Identifier: CA81689874
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs376466770
MyVariant Identifiers: chr3:g.119121227G>A (hg19) chr3:g.119402380G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119402380G>A , CM000665.2:g.119402380G>A GRCh38
NC_000003.11:g.119121227G>A , CM000665.1:g.119121227G>A GRCh37
NC_000003.10:g.120603917G>A NCBI36
NG_007665.2:g.113008G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.1628G>A MANE Select ENSP00000264245.4:p.Gly543Glu
ENST00000264245.8:c.1628G>A ENSP00000264245.4:p.Gly543Glu
NM_020754.3:c.1628G>A NP_065805.2:p.Gly543Glu
XM_005247671.3:c.1535G>A XP_005247728.1:p.Gly512Glu
XM_006713714.2:c.1568G>A XP_006713777.1:p.Gly523Glu
XM_006713714.3:c.1568G>A XP_006713777.1:p.Gly523Glu
XM_017006955.1:c.1136G>A XP_016862444.1:p.Gly379Glu
NM_020754.4:c.1628G>A MANE Select NP_065805.2:p.Gly543Glu
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