Canonical Allele Identifier: CA346226335
Gene: OSR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.19552923T>G (hg19) chr2:g.19353162T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.19353162T>G , CM000664.2:g.19353162T>G GRCh38
NC_000002.11:g.19552923T>G , CM000664.1:g.19552923T>G GRCh37
NC_000002.10:g.19416404T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000272223.3:c.644A>C MANE Select ENSP00000272223.2:p.Gln215Pro
ENST00000272223.2:c.644A>C ENSP00000272223.2:p.Gln215Pro
ENST00000487581.1:n.3751A>C
NM_145260.2:c.644A>C NP_660303.1:p.Gln215Pro
XM_006711942.2:c.644A>C XP_006712005.1:p.Gln215Pro
XM_006711942.4:c.644A>C XP_006712005.1:p.Gln215Pro
NM_145260.3:c.644A>C MANE Select NP_660303.1:p.Gln215Pro
Search 100 bp 5'
Search 100 bp 3'