Canonical Allele Identifier: CA425360187
Gene: OSR1 HGNC NCBI

Linked Data

gnomAD v4: 2-19353155-G-A
MyVariant Identifiers: chr2:g.19552916G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.19353155G>A , CM000664.2:g.19353155G>A GRCh38
NC_000002.11:g.19552916G>A , CM000664.1:g.19552916G>A GRCh37
NC_000002.10:g.19416397G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000272223.3:c.651C>T MANE Select ENSP00000272223.2:p.His217=
ENST00000272223.2:c.651C>T ENSP00000272223.2:p.His217=
ENST00000487581.1:n.3758C>T
NM_145260.2:c.651C>T NP_660303.1:p.His217=
XM_006711942.2:c.651C>T XP_006712005.1:p.His217=
XM_006711942.4:c.651C>T XP_006712005.1:p.His217=
NM_145260.3:c.651C>T MANE Select NP_660303.1:p.His217=