Canonical Allele Identifier: CA425360180
Gene: OSR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.19552904G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.19353143G>A , CM000664.2:g.19353143G>A GRCh38
NC_000002.11:g.19552904G>A , CM000664.1:g.19552904G>A GRCh37
NC_000002.10:g.19416385G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000272223.3:c.663C>T MANE Select ENSP00000272223.2:p.His221=
ENST00000272223.2:c.663C>T ENSP00000272223.2:p.His221=
ENST00000487581.1:n.3770C>T
NM_145260.2:c.663C>T NP_660303.1:p.His221=
XM_006711942.2:c.663C>T XP_006712005.1:p.His221=
XM_006711942.4:c.663C>T XP_006712005.1:p.His221=
NM_145260.3:c.663C>T MANE Select NP_660303.1:p.His221=