Canonical Allele Identifier: CA380269895

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46749667A>G (hg19) ; chr11:g.46728117A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46728117A>G , CM000673.2:g.46728117A>G	GRCh38
NC_000011.9:g.46749667A>G , CM000673.1:g.46749667A>G	GRCh37
NC_000011.8:g.46706243A>G	NCBI36
NG_008953.1:g.13925A>G , LRG_551:g.13925A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.1252A>G MANE Select	ENSP00000308541.5:p.Thr418Ala
ENST00000311907.9:c.1252A>G	ENSP00000308541.5:p.Thr418Ala
ENST00000530231.5:c.1252A>G	ENSP00000433907.1:p.Thr418Ala
NM_000506.3:c.1252A>G	NP_000497.1:p.Thr418Ala
NM_000506.4:c.1252A>G , LRG_551t1:c.1252A>G	NP_000497.1:p.Thr418Ala
NM_001311257.1:c.1204A>G	NP_001298186.1:p.Thr402Ala
XR_428840.2:n.1296A>G
XR_428840.4:n.1287A>G
NM_000506.5:c.1252A>G MANE Select	NP_000497.1:p.Thr418Ala
NM_001311257.2:c.1204A>G	NP_001298186.1:p.Thr402Ala