Canonical Allele Identifier: CA474043741

Gene: F2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726025C>T , CM000673.2:g.46726025C>T	GRCh38
NC_000011.9:g.46747575C>T , CM000673.1:g.46747575C>T	GRCh37
NC_000011.8:g.46704151C>T	NCBI36
NG_008953.1:g.11833C>T , LRG_551:g.11833C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.726C>T MANE Select	ENSP00000308541.5:p.Ala242=
ENST00000311907.9:c.726C>T	ENSP00000308541.5:p.Ala242=
ENST00000442468.1:c.696C>T	ENSP00000387413.1:p.Ala232=
ENST00000490274.1:n.506C>T
ENST00000530231.5:c.726C>T	ENSP00000433907.1:p.Ala242=
NM_000506.3:c.726C>T	NP_000497.1:p.Ala242=
NM_000506.4:c.726C>T , LRG_551t1:c.726C>T	NP_000497.1:p.Ala242=
NM_001311257.1:c.678C>T	NP_001298186.1:p.Ala226=
XR_428840.2:n.770C>T
XR_428840.4:n.761C>T
NM_000506.5:c.726C>T MANE Select	NP_000497.1:p.Ala242=
NM_001311257.2:c.678C>T	NP_001298186.1:p.Ala226=