Canonical Allele Identifier: CA393770650
Gene: MESP2 HGNC NCBI

Linked Data

gnomAD v4: 15-89776868-G-A
MyVariant Identifiers: chr15:g.90320099G>A (hg19) chr15:g.89776868G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89776868G>A , CM000677.2:g.89776868G>A GRCh38
NC_000015.9:g.90320099G>A , CM000677.1:g.90320099G>A GRCh37
NC_000015.8:g.88121103G>A NCBI36
NG_008608.1:g.5511G>A
NG_008608.2:g.21278G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000341735.5:c.511G>A MANE Select ENSP00000342392.3:p.Ala171Thr
ENST00000341735.3:c.511G>A ENSP00000342392.3:p.Ala171Thr
ENST00000558723.1:n.39-1197G>A
ENST00000560219.2:c.31-1197G>A ENSP00000452998.1:n.31-1197G>A
NM_001039958.1:c.511G>A NP_001035047.1:p.Ala171Thr
NM_001039958.2:c.511G>A MANE Select NP_001035047.1:p.Ala171Thr
Search 100 bp 5'
Search 100 bp 3'