Canonical Allele Identifier: CA380267084

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46748168G>T (hg19) ; chr11:g.46726618G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726618G>T , CM000673.2:g.46726618G>T	GRCh38
NC_000011.9:g.46748168G>T , CM000673.1:g.46748168G>T	GRCh37
NC_000011.8:g.46704744G>T	NCBI36
NG_008953.1:g.12426G>T , LRG_551:g.12426G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.995G>T MANE Select	ENSP00000308541.5:p.Gly332Val
ENST00000311907.9:c.995G>T	ENSP00000308541.5:p.Gly332Val
ENST00000442468.1:c.965G>T	ENSP00000387413.1:p.Gly322Val
ENST00000530231.5:c.995G>T	ENSP00000433907.1:p.Gly332Val
NM_000506.3:c.995G>T	NP_000497.1:p.Gly332Val
NM_000506.4:c.995G>T , LRG_551t1:c.995G>T	NP_000497.1:p.Gly332Val
NM_001311257.1:c.947G>T	NP_001298186.1:p.Gly316Val
XR_428840.2:n.1039G>T
XR_428840.4:n.1030G>T
NM_000506.5:c.995G>T MANE Select	NP_000497.1:p.Gly332Val
NM_001311257.2:c.947G>T	NP_001298186.1:p.Gly316Val