Canonical Allele Identifier: CA435411854
Gene: ARHGAP31 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.119133137T>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414290T>C , CM000665.2:g.119414290T>C GRCh38
NC_000003.11:g.119133137T>C , CM000665.1:g.119133137T>C GRCh37
NC_000003.10:g.120615827T>C NCBI36
NG_007665.2:g.124918T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2361T>C MANE Select ENSP00000264245.4:p.Pro787=
ENST00000264245.8:c.2361T>C ENSP00000264245.4:p.Pro787=
NM_020754.3:c.2361T>C NP_065805.2:p.Pro787=
XM_005247671.3:c.2268T>C XP_005247728.1:p.Pro756=
XM_006713714.2:c.2301T>C XP_006713777.1:p.Pro767=
XM_006713714.3:c.2301T>C XP_006713777.1:p.Pro767=
XM_017006955.1:c.1869T>C XP_016862444.1:p.Pro623=
NM_020754.4:c.2361T>C MANE Select NP_065805.2:p.Pro787=
Search 100 bp 5'
Search 100 bp 3'