Canonical Allele Identifier: CA473871335

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46747410C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725860C>G , CM000673.2:g.46725860C>G	GRCh38
NC_000011.9:g.46747410C>G , CM000673.1:g.46747410C>G	GRCh37
NC_000011.8:g.46703986C>G	NCBI36
NG_008953.1:g.11668C>G , LRG_551:g.11668C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000311907.10:c.561C>G MANE Select	ENSP00000308541.5:p.Gly187=
ENST00000311907.9:c.561C>G	ENSP00000308541.5:p.Gly187=
ENST00000442468.1:c.531C>G	ENSP00000387413.1:p.Gly177=
ENST00000490274.1:n.341C>G
ENST00000530231.5:c.561C>G	ENSP00000433907.1:p.Gly187=
NM_000506.3:c.561C>G	NP_000497.1:p.Gly187=
NM_000506.4:c.561C>G , LRG_551t1:c.561C>G	NP_000497.1:p.Gly187=
NM_001311257.1:c.513C>G	NP_001298186.1:p.Gly171=
XR_428840.2:n.605C>G
XR_428840.4:n.596C>G
NM_000506.5:c.561C>G MANE Select	NP_000497.1:p.Gly187=
NM_001311257.2:c.513C>G	NP_001298186.1:p.Gly171=