Canonical Allele Identifier: CA376196616
Gene: MRC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.17849740T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17849740T>A , CM000672.2:g.17849740T>A GRCh38
NG_047011.1:g.45398T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000569591.3:c.1225T>A MANE Select ENSP00000455897.1:p.Phe409Ile
ENST00000569591.2:c.1225T>A ENSP00000455897.1:p.Phe409Ile
NM_002438.3:c.1225T>A NP_002429.1:p.Phe409Ile
NM_002438.4:c.1225T>A MANE Select NP_002429.1:p.Phe409Ile
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