Canonical Allele Identifier: CA380267842

Gene: F2

Linked Data

• gnomAD v4: 11-46726780-C-A
• MyVariant Identifiers: chr11:g.46748330C>A (hg19) ; chr11:g.46726780C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726780C>A , CM000673.2:g.46726780C>A	GRCh38
NC_000011.9:g.46748330C>A , CM000673.1:g.46748330C>A	GRCh37
NC_000011.8:g.46704906C>A	NCBI36
NG_008953.1:g.12588C>A , LRG_551:g.12588C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000311907.10:c.1073C>A MANE Select	ENSP00000308541.5:p.Ser358Tyr
ENST00000311907.9:c.1073C>A	ENSP00000308541.5:p.Ser358Tyr
ENST00000530231.5:c.1073C>A	ENSP00000433907.1:p.Ser358Tyr
NM_000506.3:c.1073C>A	NP_000497.1:p.Ser358Tyr
NM_000506.4:c.1073C>A , LRG_551t1:c.1073C>A	NP_000497.1:p.Ser358Tyr
NM_001311257.1:c.1025C>A	NP_001298186.1:p.Ser342Tyr
XR_428840.2:n.1117C>A
XR_428840.4:n.1108C>A
NM_000506.5:c.1073C>A MANE Select	NP_000497.1:p.Ser358Tyr
NM_001311257.2:c.1025C>A	NP_001298186.1:p.Ser342Tyr