Canonical Allele Identifier: CA7730362
Gene: MESP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 317385
ClinVar RCV Id: RCV000348753 RCV000909848 RCV002522810 RCV003920337
dbSNP Id: rs566641514
ExAC: 15:90319773 G / A
gnomAD v2: 15-90319773-G-A
gnomAD v3: 15-89776542-G-A
gnomAD v4: 15-89776542-G-A
MyVariant Identifiers: chr15:g.90319773G>A (hg19) chr15:g.89776542G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89776542G>A , CM000677.2:g.89776542G>A GRCh38
NC_000015.9:g.90319773G>A , CM000677.1:g.90319773G>A GRCh37
NC_000015.8:g.88120777G>A NCBI36
NG_008608.1:g.5185G>A
NG_008608.2:g.20952G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000341735.5:c.185G>A MANE Select ENSP00000342392.3:p.Arg62Gln
ENST00000341735.3:c.185G>A ENSP00000342392.3:p.Arg62Gln
ENST00000558723.1:n.39-1523G>A
ENST00000560219.2:c.31-1523G>A ENSP00000452998.1:n.31-1523G>A
NM_001039958.1:c.185G>A NP_001035047.1:p.Arg62Gln
NM_001039958.2:c.185G>A MANE Select NP_001035047.1:p.Arg62Gln
Search 100 bp 5'
Search 100 bp 3'