Canonical Allele Identifier: CA380263189
Gene: F2 HGNC NCBI

Linked Data

COSMIC: COSM310978
MyVariant Identifiers: chr11:g.46745009C>A (hg19) chr11:g.46723459C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46723459C>A , CM000673.2:g.46723459C>A GRCh38
NC_000011.9:g.46745009C>A , CM000673.1:g.46745009C>A GRCh37
NC_000011.8:g.46701585C>A NCBI36
NG_008953.1:g.9267C>A , LRG_551:g.9267C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311907.10:c.500C>A MANE Select ENSP00000308541.5:p.Pro167His
ENST00000311907.9:c.500C>A ENSP00000308541.5:p.Pro167His
ENST00000442468.1:c.470C>A ENSP00000387413.1:p.Pro157His
ENST00000490274.1:n.280C>A
ENST00000530231.5:c.500C>A ENSP00000433907.1:p.Pro167His
NM_000506.3:c.500C>A NP_000497.1:p.Pro167His
NM_000506.4:c.500C>A , LRG_551t1:c.500C>A NP_000497.1:p.Pro167His
NM_001311257.1:c.452C>A NP_001298186.1:p.Pro151His
XR_428840.2:n.544C>A
XR_428840.4:n.535C>A
NM_000506.5:c.500C>A MANE Select NP_000497.1:p.Pro167His
NM_001311257.2:c.452C>A NP_001298186.1:p.Pro151His
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