Canonical Allele Identifier: CA473871023
Gene: F2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.46745004G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46723454G>T , CM000673.2:g.46723454G>T GRCh38
NC_000011.9:g.46745004G>T , CM000673.1:g.46745004G>T GRCh37
NC_000011.8:g.46701580G>T NCBI36
NG_008953.1:g.9262G>T , LRG_551:g.9262G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000311907.10:c.495G>T MANE Select ENSP00000308541.5:p.Thr165=
ENST00000311907.9:c.495G>T ENSP00000308541.5:p.Thr165=
ENST00000442468.1:c.465G>T ENSP00000387413.1:p.Thr155=
ENST00000490274.1:n.275G>T
ENST00000530231.5:c.495G>T ENSP00000433907.1:p.Thr165=
NM_000506.3:c.495G>T NP_000497.1:p.Thr165=
NM_000506.4:c.495G>T , LRG_551t1:c.495G>T NP_000497.1:p.Thr165=
NM_001311257.1:c.447G>T NP_001298186.1:p.Thr149=
XR_428840.2:n.539G>T
XR_428840.4:n.530G>T
NM_000506.5:c.495G>T MANE Select NP_000497.1:p.Thr165=
NM_001311257.2:c.447G>T NP_001298186.1:p.Thr149=