Canonical Allele Identifier: CA425360188
Gene: OSR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.19552922T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.19353161T>C , CM000664.2:g.19353161T>C GRCh38
NC_000002.11:g.19552922T>C , CM000664.1:g.19552922T>C GRCh37
NC_000002.10:g.19416403T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000272223.3:c.645A>G MANE Select ENSP00000272223.2:p.Gln215=
ENST00000272223.2:c.645A>G ENSP00000272223.2:p.Gln215=
ENST00000487581.1:n.3752A>G
NM_145260.2:c.645A>G NP_660303.1:p.Gln215=
XM_006711942.2:c.645A>G XP_006712005.1:p.Gln215=
XM_006711942.4:c.645A>G XP_006712005.1:p.Gln215=
NM_145260.3:c.645A>G MANE Select NP_660303.1:p.Gln215=
Search 100 bp 5'
Search 100 bp 3'