Canonical Allele Identifier: CA474043852

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46748334C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726784C>T , CM000673.2:g.46726784C>T	GRCh38
NC_000011.9:g.46748334C>T , CM000673.1:g.46748334C>T	GRCh37
NC_000011.8:g.46704910C>T	NCBI36
NG_008953.1:g.12592C>T , LRG_551:g.12592C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.1077C>T MANE Select	ENSP00000308541.5:p.Tyr359=
ENST00000311907.9:c.1077C>T	ENSP00000308541.5:p.Tyr359=
ENST00000530231.5:c.1077C>T	ENSP00000433907.1:p.Tyr359=
NM_000506.3:c.1077C>T	NP_000497.1:p.Tyr359=
NM_000506.4:c.1077C>T , LRG_551t1:c.1077C>T	NP_000497.1:p.Tyr359=
NM_001311257.1:c.1029C>T	NP_001298186.1:p.Tyr343=
XR_428840.2:n.1121C>T
XR_428840.4:n.1112C>T
NM_000506.5:c.1077C>T MANE Select	NP_000497.1:p.Tyr359=
NM_001311257.2:c.1029C>T	NP_001298186.1:p.Tyr343=