Canonical Allele Identifier: CA492294979
Gene: MESP2 HGNC NCBI

Linked Data

dbSNP Id: rs369681915
gnomAD v2: 15-90319906-C-G
MyVariant Identifiers: chr15:g.90319906C>G (hg19) chr15:g.89776675C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89776675C>G , CM000677.2:g.89776675C>G GRCh38
NC_000015.9:g.90319906C>G , CM000677.1:g.90319906C>G GRCh37
NC_000015.8:g.88120910C>G NCBI36
NG_008608.1:g.5318C>G
NG_008608.2:g.21085C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000341735.5:c.318C>G MANE Select ENSP00000342392.3:p.Arg106=
ENST00000341735.3:c.318C>G ENSP00000342392.3:p.Arg106=
ENST00000558723.1:n.39-1390C>G
ENST00000560219.2:c.31-1390C>G ENSP00000452998.1:n.31-1390C>G
NM_001039958.1:c.318C>G NP_001035047.1:p.Arg106=
NM_001039958.2:c.318C>G MANE Select NP_001035047.1:p.Arg106=
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