Canonical Allele Identifier: CA2554011
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs774644225
ExAC: 3:119133114 C / G
gnomAD v2: 3-119133114-C-G
gnomAD v4: 3-119414267-C-G
MyVariant Identifiers: chr3:g.119133114C>G (hg19) chr3:g.119414267C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414267C>G , CM000665.2:g.119414267C>G GRCh38
NC_000003.11:g.119133114C>G , CM000665.1:g.119133114C>G GRCh37
NC_000003.10:g.120615804C>G NCBI36
NG_007665.2:g.124895C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2338C>G MANE Select ENSP00000264245.4:p.Pro780Ala
ENST00000264245.8:c.2338C>G ENSP00000264245.4:p.Pro780Ala
NM_020754.3:c.2338C>G NP_065805.2:p.Pro780Ala
XM_005247671.3:c.2245C>G XP_005247728.1:p.Pro749Ala
XM_006713714.2:c.2278C>G XP_006713777.1:p.Pro760Ala
XM_006713714.3:c.2278C>G XP_006713777.1:p.Pro760Ala
XM_017006955.1:c.1846C>G XP_016862444.1:p.Pro616Ala
NM_020754.4:c.2338C>G MANE Select NP_065805.2:p.Pro780Ala
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