Canonical Allele Identifier: CA474043703

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46747539T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725989T>C , CM000673.2:g.46725989T>C	GRCh38
NC_000011.9:g.46747539T>C , CM000673.1:g.46747539T>C	GRCh37
NC_000011.8:g.46704115T>C	NCBI36
NG_008953.1:g.11797T>C , LRG_551:g.11797T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.690T>C MANE Select	ENSP00000308541.5:p.His230=
ENST00000311907.9:c.690T>C	ENSP00000308541.5:p.His230=
ENST00000442468.1:c.660T>C	ENSP00000387413.1:p.His220=
ENST00000490274.1:n.470T>C
ENST00000530231.5:c.690T>C	ENSP00000433907.1:p.His230=
NM_000506.3:c.690T>C	NP_000497.1:p.His230=
NM_000506.4:c.690T>C , LRG_551t1:c.690T>C	NP_000497.1:p.His230=
NM_001311257.1:c.642T>C	NP_001298186.1:p.His214=
XR_428840.2:n.734T>C
XR_428840.4:n.725T>C
NM_000506.5:c.690T>C MANE Select	NP_000497.1:p.His230=
NM_001311257.2:c.642T>C	NP_001298186.1:p.His214=