Canonical Allele Identifier: CA81697744
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs560144166
MyVariant Identifiers: chr3:g.119133252G>C (hg19) chr3:g.119414405G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414405G>C , CM000665.2:g.119414405G>C GRCh38
NC_000003.11:g.119133252G>C , CM000665.1:g.119133252G>C GRCh37
NC_000003.10:g.120615942G>C NCBI36
NG_007665.2:g.125033G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2476G>C MANE Select ENSP00000264245.4:p.Asp826His
ENST00000264245.8:c.2476G>C ENSP00000264245.4:p.Asp826His
NM_020754.3:c.2476G>C NP_065805.2:p.Asp826His
XM_005247671.3:c.2383G>C XP_005247728.1:p.Asp795His
XM_006713714.2:c.2416G>C XP_006713777.1:p.Asp806His
XM_006713714.3:c.2416G>C XP_006713777.1:p.Asp806His
XM_017006955.1:c.1984G>C XP_016862444.1:p.Asp662His
NM_020754.4:c.2476G>C MANE Select NP_065805.2:p.Asp826His
Search 100 bp 5'
Search 100 bp 3'