Canonical Allele Identifier: CA380264699

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46747433T>G (hg19) ; chr11:g.46725883T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725883T>G , CM000673.2:g.46725883T>G	GRCh38
NC_000011.9:g.46747433T>G , CM000673.1:g.46747433T>G	GRCh37
NC_000011.8:g.46704009T>G	NCBI36
NG_008953.1:g.11691T>G , LRG_551:g.11691T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.584T>G MANE Select	ENSP00000308541.5:p.Met195Arg
ENST00000311907.9:c.584T>G	ENSP00000308541.5:p.Met195Arg
ENST00000442468.1:c.554T>G	ENSP00000387413.1:p.Met185Arg
ENST00000490274.1:n.364T>G
ENST00000530231.5:c.584T>G	ENSP00000433907.1:p.Met195Arg
NM_000506.3:c.584T>G	NP_000497.1:p.Met195Arg
NM_000506.4:c.584T>G , LRG_551t1:c.584T>G	NP_000497.1:p.Met195Arg
NM_001311257.1:c.536T>G	NP_001298186.1:p.Met179Arg
XR_428840.2:n.628T>G
XR_428840.4:n.619T>G
NM_000506.5:c.584T>G MANE Select	NP_000497.1:p.Met195Arg
NM_001311257.2:c.536T>G	NP_001298186.1:p.Met179Arg