Canonical Allele Identifier: CA380266587

Gene: F2

Linked Data

• gnomAD v4: 11-46726537-A-C
• MyVariant Identifiers: chr11:g.46748087A>C (hg19) ; chr11:g.46726537A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726537A>C , CM000673.2:g.46726537A>C	GRCh38
NC_000011.9:g.46748087A>C , CM000673.1:g.46748087A>C	GRCh37
NC_000011.8:g.46704663A>C	NCBI36
NG_008953.1:g.12345A>C , LRG_551:g.12345A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.914A>C MANE Select	ENSP00000308541.5:p.Glu305Ala
ENST00000311907.9:c.914A>C	ENSP00000308541.5:p.Glu305Ala
ENST00000442468.1:c.884A>C	ENSP00000387413.1:p.Glu295Ala
ENST00000530231.5:c.914A>C	ENSP00000433907.1:p.Glu305Ala
NM_000506.3:c.914A>C	NP_000497.1:p.Glu305Ala
NM_000506.4:c.914A>C , LRG_551t1:c.914A>C	NP_000497.1:p.Glu305Ala
NM_001311257.1:c.866A>C	NP_001298186.1:p.Glu289Ala
XR_428840.2:n.958A>C
XR_428840.4:n.949A>C
NM_000506.5:c.914A>C MANE Select	NP_000497.1:p.Glu305Ala
NM_001311257.2:c.866A>C	NP_001298186.1:p.Glu289Ala