Canonical Allele Identifier: CA13460889

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46719945C>T , CM000673.2:g.46719945C>T	GRCh38
NC_000011.9:g.46741495C>T , CM000673.1:g.46741495C>T	GRCh37
NC_000011.8:g.46698071C>T	NCBI36
NG_008953.1:g.5753C>T , LRG_551:g.5753C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000506.5:c.240+83C>T MANE Select	NP_000497.1:n.240+83C>T
ENST00000311907.10:c.240+83C>T MANE Select	ENSP00000308541.5:n.240+83C>T
NM_000506.3:c.240+83C>T	NP_000497.1:n.240+83C>T
NM_000506.4:c.240+83C>T , LRG_551t1:c.240+83C>T	NP_000497.1:n.240+83C>T
NM_001311257.1:c.192+83C>T	NP_001298186.1:n.192+83C>T
NM_001311257.2:c.192+83C>T	NP_001298186.1:n.192+83C>T
ENST00000311907.9:c.240+83C>T	ENSP00000308541.5:n.240+83C>T
ENST00000442468.1:c.210+83C>T	ENSP00000387413.1:n.210+83C>T
ENST00000469189.1:n.363C>T
ENST00000530231.5:c.240+83C>T	ENSP00000433907.1:n.240+83C>T
XR_428840.2:n.284+83C>T
XR_428840.4:n.275+83C>T