Canonical Allele Identifier: CA435411407

Gene: ARHGAP31

Linked Data

• dbSNP Id: rs1236282842
• gnomAD v2: 3-119132723-T-C
• gnomAD v3: 3-119413876-T-C
• gnomAD v4: 3-119413876-T-C
• MyVariant Identifiers: chr3:g.119132723T>C (hg19) ; chr3:g.119413876T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413876T>C , CM000665.2:g.119413876T>C	GRCh38
NC_000003.11:g.119132723T>C , CM000665.1:g.119132723T>C	GRCh37
NC_000003.10:g.120615413T>C	NCBI36
NG_007665.2:g.124504T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264245.9:c.1947T>C MANE Select	ENSP00000264245.4:p.Asn649=
ENST00000264245.8:c.1947T>C	ENSP00000264245.4:p.Asn649=
NM_020754.3:c.1947T>C	NP_065805.2:p.Asn649=
XM_005247671.3:c.1854T>C	XP_005247728.1:p.Asn618=
XM_006713714.2:c.1887T>C	XP_006713777.1:p.Asn629=
XM_006713714.3:c.1887T>C	XP_006713777.1:p.Asn629=
XM_017006955.1:c.1455T>C	XP_016862444.1:p.Asn485=
NM_020754.4:c.1947T>C MANE Select	NP_065805.2:p.Asn649=