Canonical Allele Identifier: CA354050466
Gene: ARHGAP31 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.119133088T>A (hg19) chr3:g.119414241T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414241T>A , CM000665.2:g.119414241T>A GRCh38
NC_000003.11:g.119133088T>A , CM000665.1:g.119133088T>A GRCh37
NC_000003.10:g.120615778T>A NCBI36
NG_007665.2:g.124869T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2312T>A MANE Select ENSP00000264245.4:p.Val771Glu
ENST00000264245.8:c.2312T>A ENSP00000264245.4:p.Val771Glu
NM_020754.3:c.2312T>A NP_065805.2:p.Val771Glu
XM_005247671.3:c.2219T>A XP_005247728.1:p.Val740Glu
XM_006713714.2:c.2252T>A XP_006713777.1:p.Val751Glu
XM_006713714.3:c.2252T>A XP_006713777.1:p.Val751Glu
XM_017006955.1:c.1820T>A XP_016862444.1:p.Val607Glu
NM_020754.4:c.2312T>A MANE Select NP_065805.2:p.Val771Glu
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