Canonical Allele Identifier: CA346226295
Gene: OSR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.19552906G>C (hg19) chr2:g.19353145G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.19353145G>C , CM000664.2:g.19353145G>C GRCh38
NC_000002.11:g.19552906G>C , CM000664.1:g.19552906G>C GRCh37
NC_000002.10:g.19416387G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272223.3:c.661C>G MANE Select ENSP00000272223.2:p.His221Asp
ENST00000272223.2:c.661C>G ENSP00000272223.2:p.His221Asp
ENST00000487581.1:n.3768C>G
NM_145260.2:c.661C>G NP_660303.1:p.His221Asp
XM_006711942.2:c.661C>G XP_006712005.1:p.His221Asp
XM_006711942.4:c.661C>G XP_006712005.1:p.His221Asp
NM_145260.3:c.661C>G MANE Select NP_660303.1:p.His221Asp
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Search 100 bp 3'