Canonical Allele Identifier: CA354050682
Gene: ARHGAP31 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.119133123C>A (hg19) chr3:g.119414276C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414276C>A , CM000665.2:g.119414276C>A GRCh38
NC_000003.11:g.119133123C>A , CM000665.1:g.119133123C>A GRCh37
NC_000003.10:g.120615813C>A NCBI36
NG_007665.2:g.124904C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2347C>A MANE Select ENSP00000264245.4:p.Pro783Thr
ENST00000264245.8:c.2347C>A ENSP00000264245.4:p.Pro783Thr
NM_020754.3:c.2347C>A NP_065805.2:p.Pro783Thr
XM_005247671.3:c.2254C>A XP_005247728.1:p.Pro752Thr
XM_006713714.2:c.2287C>A XP_006713777.1:p.Pro763Thr
XM_006713714.3:c.2287C>A XP_006713777.1:p.Pro763Thr
XM_017006955.1:c.1855C>A XP_016862444.1:p.Pro619Thr
NM_020754.4:c.2347C>A MANE Select NP_065805.2:p.Pro783Thr
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