Canonical Allele Identifier: CA129505
Gene: ARHGAP31 HGNC NCBI

Linked Data

ClinVar Variation Id: 30857
ClinVar RCV Id: RCV000023842
dbSNP Id: rs387907031

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413976C>T , CM000665.2:g.119413976C>T GRCh38
NC_000003.11:g.119132823C>T , CM000665.1:g.119132823C>T GRCh37
NC_000003.10:g.120615513C>T NCBI36
NG_007665.2:g.124604C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264245.9:c.2047C>T MANE Select ENSP00000264245.4:p.Gln683Ter
ENST00000264245.8:c.2047C>T ENSP00000264245.4:p.Gln683Ter
NM_020754.3:c.2047C>T NP_065805.2:p.Gln683Ter
XM_005247671.3:c.1954C>T XP_005247728.1:p.Gln652Ter
XM_006713714.2:c.1987C>T XP_006713777.1:p.Gln663Ter
XM_006713714.3:c.1987C>T XP_006713777.1:p.Gln663Ter
XM_017006955.1:c.1555C>T XP_016862444.1:p.Gln519Ter
NM_020754.4:c.2047C>T MANE Select NP_065805.2:p.Gln683Ter