Canonical Allele Identifier: CA221652515

Gene: F2

Linked Data

• dbSNP Id: rs539368733
• gnomAD v3: 11-46726300-G-A
• gnomAD v4: 11-46726300-G-A
• MyVariant Identifiers: chr11:g.46747850G>A (hg19) ; chr11:g.46726300G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726300G>A , CM000673.2:g.46726300G>A	GRCh38
NC_000011.9:g.46747850G>A , CM000673.1:g.46747850G>A	GRCh37
NC_000011.8:g.46704426G>A	NCBI36
NG_008953.1:g.12108G>A , LRG_551:g.12108G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.874+127G>A MANE Select	ENSP00000308541.5:n.874+127G>A
ENST00000311907.9:c.874+127G>A	ENSP00000308541.5:n.874+127G>A
ENST00000442468.1:c.844+127G>A	ENSP00000387413.1:n.844+127G>A
ENST00000530231.5:c.874+127G>A	ENSP00000433907.1:n.874+127G>A
NM_000506.3:c.874+127G>A	NP_000497.1:n.874+127G>A
NM_000506.4:c.874+127G>A , LRG_551t1:c.874+127G>A	NP_000497.1:n.874+127G>A
NM_001311257.1:c.826+127G>A	NP_001298186.1:n.826+127G>A
XR_428840.2:n.918+127G>A
XR_428840.4:n.909+127G>A
NM_000506.5:c.874+127G>A MANE Select	NP_000497.1:n.874+127G>A
NM_001311257.2:c.826+127G>A	NP_001298186.1:n.826+127G>A