Canonical Allele Identifier: CA354048467
Gene: ARHGAP31 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.119132812C>A (hg19) chr3:g.119413965C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413965C>A , CM000665.2:g.119413965C>A GRCh38
NC_000003.11:g.119132812C>A , CM000665.1:g.119132812C>A GRCh37
NC_000003.10:g.120615502C>A NCBI36
NG_007665.2:g.124593C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2036C>A MANE Select ENSP00000264245.4:p.Thr679Asn
ENST00000264245.8:c.2036C>A ENSP00000264245.4:p.Thr679Asn
NM_020754.3:c.2036C>A NP_065805.2:p.Thr679Asn
XM_005247671.3:c.1943C>A XP_005247728.1:p.Thr648Asn
XM_006713714.2:c.1976C>A XP_006713777.1:p.Thr659Asn
XM_006713714.3:c.1976C>A XP_006713777.1:p.Thr659Asn
XM_017006955.1:c.1544C>A XP_016862444.1:p.Thr515Asn
NM_020754.4:c.2036C>A MANE Select NP_065805.2:p.Thr679Asn
Search 100 bp 5'
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