Canonical Allele Identifier: CA380267696

Gene: F2

Linked Data

• gnomAD v4: 11-46726764-A-G
• MyVariant Identifiers: chr11:g.46748314A>G (hg19) ; chr11:g.46726764A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726764A>G , CM000673.2:g.46726764A>G	GRCh38
NC_000011.9:g.46748314A>G , CM000673.1:g.46748314A>G	GRCh37
NC_000011.8:g.46704890A>G	NCBI36
NG_008953.1:g.12572A>G , LRG_551:g.12572A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000311907.10:c.1057A>G MANE Select	ENSP00000308541.5:p.Arg353Gly
ENST00000311907.9:c.1057A>G	ENSP00000308541.5:p.Arg353Gly
ENST00000530231.5:c.1057A>G	ENSP00000433907.1:p.Arg353Gly
NM_000506.3:c.1057A>G	NP_000497.1:p.Arg353Gly
NM_000506.4:c.1057A>G , LRG_551t1:c.1057A>G	NP_000497.1:p.Arg353Gly
NM_001311257.1:c.1009A>G	NP_001298186.1:p.Arg337Gly
XR_428840.2:n.1101A>G
XR_428840.4:n.1092A>G
NM_000506.5:c.1057A>G MANE Select	NP_000497.1:p.Arg353Gly
NM_001311257.2:c.1009A>G	NP_001298186.1:p.Arg337Gly