Canonical Allele Identifier: CA346226351
Gene: OSR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.19552931G>T (hg19) chr2:g.19353170G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.19353170G>T , CM000664.2:g.19353170G>T GRCh38
NC_000002.11:g.19552931G>T , CM000664.1:g.19552931G>T GRCh37
NC_000002.10:g.19416412G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272223.3:c.636C>A MANE Select ENSP00000272223.2:p.Phe212Leu
ENST00000272223.2:c.636C>A ENSP00000272223.2:p.Phe212Leu
ENST00000487581.1:n.3743C>A
NM_145260.2:c.636C>A NP_660303.1:p.Phe212Leu
XM_006711942.2:c.636C>A XP_006712005.1:p.Phe212Leu
XM_006711942.4:c.636C>A XP_006712005.1:p.Phe212Leu
NM_145260.3:c.636C>A MANE Select NP_660303.1:p.Phe212Leu
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