Canonical Allele Identifier: CA354049607

Gene: ARHGAP31

Linked Data

• MyVariant Identifiers: chr3:g.119132951G>T (hg19) ; chr3:g.119414104G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119414104G>T , CM000665.2:g.119414104G>T	GRCh38
NC_000003.11:g.119132951G>T , CM000665.1:g.119132951G>T	GRCh37
NC_000003.10:g.120615641G>T	NCBI36
NG_007665.2:g.124732G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2175G>T MANE Select	ENSP00000264245.4:p.Gln725His
ENST00000264245.8:c.2175G>T	ENSP00000264245.4:p.Gln725His
NM_020754.3:c.2175G>T	NP_065805.2:p.Gln725His
XM_005247671.3:c.2082G>T	XP_005247728.1:p.Gln694His
XM_006713714.2:c.2115G>T	XP_006713777.1:p.Gln705His
XM_006713714.3:c.2115G>T	XP_006713777.1:p.Gln705His
XM_017006955.1:c.1683G>T	XP_016862444.1:p.Gln561His
NM_020754.4:c.2175G>T MANE Select	NP_065805.2:p.Gln725His