Canonical Allele Identifier: CA474043382

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46747440A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725890A>C , CM000673.2:g.46725890A>C	GRCh38
NC_000011.9:g.46747440A>C , CM000673.1:g.46747440A>C	GRCh37
NC_000011.8:g.46704016A>C	NCBI36
NG_008953.1:g.11698A>C , LRG_551:g.11698A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.591A>C MANE Select	ENSP00000308541.5:p.Pro197=
ENST00000311907.9:c.591A>C	ENSP00000308541.5:p.Pro197=
ENST00000442468.1:c.561A>C	ENSP00000387413.1:p.Pro187=
ENST00000490274.1:n.371A>C
ENST00000530231.5:c.591A>C	ENSP00000433907.1:p.Pro197=
NM_000506.3:c.591A>C	NP_000497.1:p.Pro197=
NM_000506.4:c.591A>C , LRG_551t1:c.591A>C	NP_000497.1:p.Pro197=
NM_001311257.1:c.543A>C	NP_001298186.1:p.Pro181=
XR_428840.2:n.635A>C
XR_428840.4:n.626A>C
NM_000506.5:c.591A>C MANE Select	NP_000497.1:p.Pro197=
NM_001311257.2:c.543A>C	NP_001298186.1:p.Pro181=