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Canonical Allele Identifier:
CA1873787750
Community Standard Title: NM_000607.4(ORM1):c.113G= (p.Arg38=)
Gene: ORM1
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.114323246G= , CM000671.2:g.114323246G=
GRCh38
NC_000009.11:g.117085526G= , CM000671.1:g.117085526G=
GRCh37
NC_000009.10:g.116125347G=
NCBI36
NG_012108.1:g.5224G=
Transcript Alleles
HGVS
Amino-acid Change
NM_000607.4:c.113G=
MANE Select
NP_000598.2:p.Arg38=
ENST00000259396.9:c.113G=
MANE Select
ENSP00000259396.8:p.Arg38=
NM_000607.2:c.113G=
NP_000598.2:p.Arg38=
NM_000607.3:c.113G=
NP_000598.2:p.Arg38=
ENST00000259396.8:c.113G=
ENSP00000259396.8:p.Arg38=
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