Canonical Allele Identifier: CA1969073828
Gene: F2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46727855C= , CM000673.2:g.46727855C= GRCh38
NC_000011.9:g.46749405C= , CM000673.1:g.46749405C= GRCh37
NC_000011.8:g.46705981C= NCBI36
NG_008953.1:g.13663C= , LRG_551:g.13663C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311907.10:c.1131-141C= MANE Select ENSP00000308541.5:n.1131-141C=
ENST00000311907.9:c.1131-141C= ENSP00000308541.5:n.1131-141C=
ENST00000530231.5:c.1131-141C= ENSP00000433907.1:n.1131-141C=
NM_000506.3:c.1131-141C= NP_000497.1:n.1131-141C=
NM_000506.4:c.1131-141C= , LRG_551t1:c.1131-141C= NP_000497.1:n.1131-141C=
NM_001311257.1:c.1083-141C= NP_001298186.1:n.1083-141C=
XR_428840.2:n.1175-141C=
XR_428840.4:n.1166-141C=
NM_000506.5:c.1131-141C= MANE Select NP_000497.1:n.1131-141C=
NM_001311257.2:c.1083-141C= NP_001298186.1:n.1083-141C=
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