Canonical Allele Identifier: CA2554015
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs186621177
ExAC: 3:119133135 C / T
gnomAD v2: 3-119133135-C-T
gnomAD v3: 3-119414288-C-T
gnomAD v4: 3-119414288-C-T
MyVariant Identifiers: chr3:g.119133135C>T (hg19) chr3:g.119414288C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414288C>T , CM000665.2:g.119414288C>T GRCh38
NC_000003.11:g.119133135C>T , CM000665.1:g.119133135C>T GRCh37
NC_000003.10:g.120615825C>T NCBI36
NG_007665.2:g.124916C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2359C>T MANE Select ENSP00000264245.4:p.Pro787Ser
ENST00000264245.8:c.2359C>T ENSP00000264245.4:p.Pro787Ser
NM_020754.3:c.2359C>T NP_065805.2:p.Pro787Ser
XM_005247671.3:c.2266C>T XP_005247728.1:p.Pro756Ser
XM_006713714.2:c.2299C>T XP_006713777.1:p.Pro767Ser
XM_006713714.3:c.2299C>T XP_006713777.1:p.Pro767Ser
XM_017006955.1:c.1867C>T XP_016862444.1:p.Pro623Ser
NM_020754.4:c.2359C>T MANE Select NP_065805.2:p.Pro787Ser
Search 100 bp 5'
Search 100 bp 3'