Canonical Allele Identifier: CA2574810818

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726667C>T , CM000673.2:g.46726667C>T	GRCh38
NC_000011.9:g.46748217C>T , CM000673.1:g.46748217C>T	GRCh37
NC_000011.8:g.46704793C>T	NCBI36
NG_008953.1:g.12475C>T , LRG_551:g.12475C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000311907.10:c.1003+41C>T MANE Select	ENSP00000308541.5:n.1003+41C>T
ENST00000311907.9:c.1003+41C>T	ENSP00000308541.5:n.1003+41C>T
ENST00000530231.5:c.1003+41C>T	ENSP00000433907.1:n.1003+41C>T
NM_000506.3:c.1003+41C>T	NP_000497.1:n.1003+41C>T
NM_000506.4:c.1003+41C>T , LRG_551t1:c.1003+41C>T	NP_000497.1:n.1003+41C>T
NM_001311257.1:c.955+41C>T	NP_001298186.1:n.955+41C>T
XR_428840.2:n.1047+41C>T
XR_428840.4:n.1038+41C>T
NM_000506.5:c.1003+41C>T MANE Select	NP_000497.1:n.1003+41C>T
NM_001311257.2:c.955+41C>T	NP_001298186.1:n.955+41C>T