Canonical Allele Identifier: CA393770085
Gene: MESP2 HGNC NCBI

Linked Data

dbSNP Id: rs1199258857
gnomAD v3: 15-89776770-T-C
gnomAD v4: 15-89776770-T-C
MyVariant Identifiers: chr15:g.90320001T>C (hg19) chr15:g.89776770T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89776770T>C , CM000677.2:g.89776770T>C GRCh38
NC_000015.9:g.90320001T>C , CM000677.1:g.90320001T>C GRCh37
NC_000015.8:g.88121005T>C NCBI36
NG_008608.1:g.5413T>C
NG_008608.2:g.21180T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000341735.5:c.413T>C MANE Select ENSP00000342392.3:p.Val138Ala
ENST00000341735.3:c.413T>C ENSP00000342392.3:p.Val138Ala
ENST00000558723.1:n.39-1295T>C
ENST00000560219.2:c.31-1295T>C ENSP00000452998.1:n.31-1295T>C
NM_001039958.1:c.413T>C NP_001035047.1:p.Val138Ala
NM_001039958.2:c.413T>C MANE Select NP_001035047.1:p.Val138Ala
Search 100 bp 5'
Search 100 bp 3'