Canonical Allele Identifier: CA380269062

Gene: F2

Linked Data

• gnomAD v4: 11-46728000-G-A
• MyVariant Identifiers: chr11:g.46749550G>A (hg19) ; chr11:g.46728000G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46728000G>A , CM000673.2:g.46728000G>A	GRCh38
NC_000011.9:g.46749550G>A , CM000673.1:g.46749550G>A	GRCh37
NC_000011.8:g.46706126G>A	NCBI36
NG_008953.1:g.13808G>A , LRG_551:g.13808G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.1135G>A MANE Select	ENSP00000308541.5:p.Val379Met
ENST00000311907.9:c.1135G>A	ENSP00000308541.5:p.Val379Met
ENST00000530231.5:c.1135G>A	ENSP00000433907.1:p.Val379Met
NM_000506.3:c.1135G>A	NP_000497.1:p.Val379Met
NM_000506.4:c.1135G>A , LRG_551t1:c.1135G>A	NP_000497.1:p.Val379Met
NM_001311257.1:c.1087G>A	NP_001298186.1:p.Val363Met
XR_428840.2:n.1179G>A
XR_428840.4:n.1170G>A
NM_000506.5:c.1135G>A MANE Select	NP_000497.1:p.Val379Met
NM_001311257.2:c.1087G>A	NP_001298186.1:p.Val363Met