Canonical Allele Identifier: CA435411800
Gene: ARHGAP31 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.119133113T>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414266T>C , CM000665.2:g.119414266T>C GRCh38
NC_000003.11:g.119133113T>C , CM000665.1:g.119133113T>C GRCh37
NC_000003.10:g.120615803T>C NCBI36
NG_007665.2:g.124894T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2337T>C MANE Select ENSP00000264245.4:p.Pro779=
ENST00000264245.8:c.2337T>C ENSP00000264245.4:p.Pro779=
NM_020754.3:c.2337T>C NP_065805.2:p.Pro779=
XM_005247671.3:c.2244T>C XP_005247728.1:p.Pro748=
XM_006713714.2:c.2277T>C XP_006713777.1:p.Pro759=
XM_006713714.3:c.2277T>C XP_006713777.1:p.Pro759=
XM_017006955.1:c.1845T>C XP_016862444.1:p.Pro615=
NM_020754.4:c.2337T>C MANE Select NP_065805.2:p.Pro779=
Search 100 bp 5'
Search 100 bp 3'