Canonical Allele Identifier: CA2554048
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs746663829

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414408A>G , CM000665.2:g.119414408A>G GRCh38
NC_000003.11:g.119133255A>G , CM000665.1:g.119133255A>G GRCh37
NC_000003.10:g.120615945A>G NCBI36
NG_007665.2:g.125036A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2479A>G MANE Select ENSP00000264245.4:p.Ser827Gly
ENST00000264245.8:c.2479A>G ENSP00000264245.4:p.Ser827Gly
NM_020754.3:c.2479A>G NP_065805.2:p.Ser827Gly
XM_005247671.3:c.2386A>G XP_005247728.1:p.Ser796Gly
XM_006713714.2:c.2419A>G XP_006713777.1:p.Ser807Gly
XM_006713714.3:c.2419A>G XP_006713777.1:p.Ser807Gly
XM_017006955.1:c.1987A>G XP_016862444.1:p.Ser663Gly
NM_020754.4:c.2479A>G MANE Select NP_065805.2:p.Ser827Gly