Canonical Allele Identifier: CA354050748
Gene: ARHGAP31 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.119133130C>A (hg19) chr3:g.119414283C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414283C>A , CM000665.2:g.119414283C>A GRCh38
NC_000003.11:g.119133130C>A , CM000665.1:g.119133130C>A GRCh37
NC_000003.10:g.120615820C>A NCBI36
NG_007665.2:g.124911C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2354C>A MANE Select ENSP00000264245.4:p.Pro785His
ENST00000264245.8:c.2354C>A ENSP00000264245.4:p.Pro785His
NM_020754.3:c.2354C>A NP_065805.2:p.Pro785His
XM_005247671.3:c.2261C>A XP_005247728.1:p.Pro754His
XM_006713714.2:c.2294C>A XP_006713777.1:p.Pro765His
XM_006713714.3:c.2294C>A XP_006713777.1:p.Pro765His
XM_017006955.1:c.1862C>A XP_016862444.1:p.Pro621His
NM_020754.4:c.2354C>A MANE Select NP_065805.2:p.Pro785His
Search 100 bp 5'
Search 100 bp 3'