Canonical Allele Identifier: CA380262806
Gene: F2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.46744930A>G (hg19) chr11:g.46723380A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46723380A>G , CM000673.2:g.46723380A>G GRCh38
NC_000011.9:g.46744930A>G , CM000673.1:g.46744930A>G GRCh37
NC_000011.8:g.46701506A>G NCBI36
NG_008953.1:g.9188A>G , LRG_551:g.9188A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000311907.10:c.423-2A>G MANE Select ENSP00000308541.5:n.423-2A>G
ENST00000311907.9:c.423-2A>G ENSP00000308541.5:n.423-2A>G
ENST00000442468.1:c.393-2A>G ENSP00000387413.1:n.393-2A>G
ENST00000490274.1:n.201A>G
ENST00000530231.5:c.423-2A>G ENSP00000433907.1:n.423-2A>G
NM_000506.3:c.423-2A>G NP_000497.1:n.423-2A>G
NM_000506.4:c.423-2A>G , LRG_551t1:c.423-2A>G NP_000497.1:n.423-2A>G
NM_001311257.1:c.375-2A>G NP_001298186.1:n.375-2A>G
XR_428840.2:n.467-2A>G
XR_428840.4:n.458-2A>G
NM_000506.5:c.423-2A>G MANE Select NP_000497.1:n.423-2A>G
NM_001311257.2:c.375-2A>G NP_001298186.1:n.375-2A>G
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