Canonical Allele Identifier: CA380265214

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46747578G>C (hg19) ; chr11:g.46726028G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726028G>C , CM000673.2:g.46726028G>C	GRCh38
NC_000011.9:g.46747578G>C , CM000673.1:g.46747578G>C	GRCh37
NC_000011.8:g.46704154G>C	NCBI36
NG_008953.1:g.11836G>C , LRG_551:g.11836G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.729G>C MANE Select	ENSP00000308541.5:p.Lys243Asn
ENST00000311907.9:c.729G>C	ENSP00000308541.5:p.Lys243Asn
ENST00000442468.1:c.699G>C	ENSP00000387413.1:p.Lys233Asn
ENST00000490274.1:n.509G>C
ENST00000530231.5:c.729G>C	ENSP00000433907.1:p.Lys243Asn
NM_000506.3:c.729G>C	NP_000497.1:p.Lys243Asn
NM_000506.4:c.729G>C , LRG_551t1:c.729G>C	NP_000497.1:p.Lys243Asn
NM_001311257.1:c.681G>C	NP_001298186.1:p.Lys227Asn
XR_428840.2:n.773G>C
XR_428840.4:n.764G>C
NM_000506.5:c.729G>C MANE Select	NP_000497.1:p.Lys243Asn
NM_001311257.2:c.681G>C	NP_001298186.1:p.Lys227Asn