Canonical Allele Identifier: CA474043792

Gene: F2

Linked Data

• gnomAD v4: 11-46726115-G-T
• MyVariant Identifiers: chr11:g.46747665G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726115G>T , CM000673.2:g.46726115G>T	GRCh38
NC_000011.9:g.46747665G>T , CM000673.1:g.46747665G>T	GRCh37
NC_000011.8:g.46704241G>T	NCBI36
NG_008953.1:g.11923G>T , LRG_551:g.11923G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.816G>T MANE Select	ENSP00000308541.5:p.Val272=
ENST00000311907.9:c.816G>T	ENSP00000308541.5:p.Val272=
ENST00000442468.1:c.786G>T	ENSP00000387413.1:p.Val262=
ENST00000530231.5:c.816G>T	ENSP00000433907.1:p.Val272=
NM_000506.3:c.816G>T	NP_000497.1:p.Val272=
NM_000506.4:c.816G>T , LRG_551t1:c.816G>T	NP_000497.1:p.Val272=
NM_001311257.1:c.768G>T	NP_001298186.1:p.Val256=
XR_428840.2:n.860G>T
XR_428840.4:n.851G>T
NM_000506.5:c.816G>T MANE Select	NP_000497.1:p.Val272=
NM_001311257.2:c.768G>T	NP_001298186.1:p.Val256=