Canonical Allele Identifier: CA393770376
Gene: MESP2 HGNC NCBI

Linked Data

dbSNP Id: rs1357972278
gnomAD v2: 15-90320054-G-A
gnomAD v3: 15-89776823-G-A
gnomAD v4: 15-89776823-G-A
MyVariant Identifiers: chr15:g.90320054G>A (hg19) chr15:g.89776823G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89776823G>A , CM000677.2:g.89776823G>A GRCh38
NC_000015.9:g.90320054G>A , CM000677.1:g.90320054G>A GRCh37
NC_000015.8:g.88121058G>A NCBI36
NG_008608.1:g.5466G>A
NG_008608.2:g.21233G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000341735.5:c.466G>A MANE Select ENSP00000342392.3:p.Ala156Thr
ENST00000341735.3:c.466G>A ENSP00000342392.3:p.Ala156Thr
ENST00000558723.1:n.39-1242G>A
ENST00000560219.2:c.31-1242G>A ENSP00000452998.1:n.31-1242G>A
NM_001039958.1:c.466G>A NP_001035047.1:p.Ala156Thr
NM_001039958.2:c.466G>A MANE Select NP_001035047.1:p.Ala156Thr
Search 100 bp 5'
Search 100 bp 3'