Canonical Allele Identifier: CA380264688

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46747427T>G (hg19) ; chr11:g.46725877T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725877T>G , CM000673.2:g.46725877T>G	GRCh38
NC_000011.9:g.46747427T>G , CM000673.1:g.46747427T>G	GRCh37
NC_000011.8:g.46704003T>G	NCBI36
NG_008953.1:g.11685T>G , LRG_551:g.11685T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.578T>G MANE Select	ENSP00000308541.5:p.Val193Gly
ENST00000311907.9:c.578T>G	ENSP00000308541.5:p.Val193Gly
ENST00000442468.1:c.548T>G	ENSP00000387413.1:p.Val183Gly
ENST00000490274.1:n.358T>G
ENST00000530231.5:c.578T>G	ENSP00000433907.1:p.Val193Gly
NM_000506.3:c.578T>G	NP_000497.1:p.Val193Gly
NM_000506.4:c.578T>G , LRG_551t1:c.578T>G	NP_000497.1:p.Val193Gly
NM_001311257.1:c.530T>G	NP_001298186.1:p.Val177Gly
XR_428840.2:n.622T>G
XR_428840.4:n.613T>G
NM_000506.5:c.578T>G MANE Select	NP_000497.1:p.Val193Gly
NM_001311257.2:c.530T>G	NP_001298186.1:p.Val177Gly