Canonical Allele Identifier: CA380264969

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46747515G>T (hg19) ; chr11:g.46725965G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725965G>T , CM000673.2:g.46725965G>T	GRCh38
NC_000011.9:g.46747515G>T , CM000673.1:g.46747515G>T	GRCh37
NC_000011.8:g.46704091G>T	NCBI36
NG_008953.1:g.11773G>T , LRG_551:g.11773G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.666G>T MANE Select	ENSP00000308541.5:p.Gln222His
ENST00000311907.9:c.666G>T	ENSP00000308541.5:p.Gln222His
ENST00000442468.1:c.636G>T	ENSP00000387413.1:p.Gln212His
ENST00000490274.1:n.446G>T
ENST00000530231.5:c.666G>T	ENSP00000433907.1:p.Gln222His
NM_000506.3:c.666G>T	NP_000497.1:p.Gln222His
NM_000506.4:c.666G>T , LRG_551t1:c.666G>T	NP_000497.1:p.Gln222His
NM_001311257.1:c.618G>T	NP_001298186.1:p.Gln206His
XR_428840.2:n.710G>T
XR_428840.4:n.701G>T
NM_000506.5:c.666G>T MANE Select	NP_000497.1:p.Gln222His
NM_001311257.2:c.618G>T	NP_001298186.1:p.Gln206His