Canonical Allele Identifier: CA474043738

Gene: F2

Linked Data

• gnomAD v4: 11-46726019-A-G
• MyVariant Identifiers: chr11:g.46747569A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726019A>G , CM000673.2:g.46726019A>G	GRCh38
NC_000011.9:g.46747569A>G , CM000673.1:g.46747569A>G	GRCh37
NC_000011.8:g.46704145A>G	NCBI36
NG_008953.1:g.11827A>G , LRG_551:g.11827A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.720A>G MANE Select	ENSP00000308541.5:p.Ala240=
ENST00000311907.9:c.720A>G	ENSP00000308541.5:p.Ala240=
ENST00000442468.1:c.690A>G	ENSP00000387413.1:p.Ala230=
ENST00000490274.1:n.500A>G
ENST00000530231.5:c.720A>G	ENSP00000433907.1:p.Ala240=
NM_000506.3:c.720A>G	NP_000497.1:p.Ala240=
NM_000506.4:c.720A>G , LRG_551t1:c.720A>G	NP_000497.1:p.Ala240=
NM_001311257.1:c.672A>G	NP_001298186.1:p.Ala224=
XR_428840.2:n.764A>G
XR_428840.4:n.755A>G
NM_000506.5:c.720A>G MANE Select	NP_000497.1:p.Ala240=
NM_001311257.2:c.672A>G	NP_001298186.1:p.Ala224=