Canonical Allele Identifier: CA473871862

Gene: F2

Linked Data

• gnomAD v4: 11-46728074-C-A
• MyVariant Identifiers: chr11:g.46749624C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46728074C>A , CM000673.2:g.46728074C>A	GRCh38
NC_000011.9:g.46749624C>A , CM000673.1:g.46749624C>A	GRCh37
NC_000011.8:g.46706200C>A	NCBI36
NG_008953.1:g.13882C>A , LRG_551:g.13882C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.1209C>A MANE Select	ENSP00000308541.5:p.Thr403=
ENST00000311907.9:c.1209C>A	ENSP00000308541.5:p.Thr403=
ENST00000530231.5:c.1209C>A	ENSP00000433907.1:p.Thr403=
NM_000506.3:c.1209C>A	NP_000497.1:p.Thr403=
NM_000506.4:c.1209C>A , LRG_551t1:c.1209C>A	NP_000497.1:p.Thr403=
NM_001311257.1:c.1161C>A	NP_001298186.1:p.Thr387=
XR_428840.2:n.1253C>A
XR_428840.4:n.1244C>A
NM_000506.5:c.1209C>A MANE Select	NP_000497.1:p.Thr403=
NM_001311257.2:c.1161C>A	NP_001298186.1:p.Thr387=