Canonical Allele Identifier: CA81697334

Gene: ARHGAP31

Linked Data

• dbSNP Id: rs371951976
• gnomAD v3: 3-119413970-C-T
• gnomAD v4: 3-119413970-C-T
• MyVariant Identifiers: chr3:g.119132817C>T (hg19) ; chr3:g.119413970C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119413970C>T , CM000665.2:g.119413970C>T	GRCh38
NC_000003.11:g.119132817C>T , CM000665.1:g.119132817C>T	GRCh37
NC_000003.10:g.120615507C>T	NCBI36
NG_007665.2:g.124598C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.2041C>T MANE Select	ENSP00000264245.4:p.Pro681Ser
ENST00000264245.8:c.2041C>T	ENSP00000264245.4:p.Pro681Ser
NM_020754.3:c.2041C>T	NP_065805.2:p.Pro681Ser
XM_005247671.3:c.1948C>T	XP_005247728.1:p.Pro650Ser
XM_006713714.2:c.1981C>T	XP_006713777.1:p.Pro661Ser
XM_006713714.3:c.1981C>T	XP_006713777.1:p.Pro661Ser
XM_017006955.1:c.1549C>T	XP_016862444.1:p.Pro517Ser
NM_020754.4:c.2041C>T MANE Select	NP_065805.2:p.Pro681Ser