Canonical Allele Identifier: CA380264899

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46747495G>T (hg19) ; chr11:g.46725945G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725945G>T , CM000673.2:g.46725945G>T	GRCh38
NC_000011.9:g.46747495G>T , CM000673.1:g.46747495G>T	GRCh37
NC_000011.8:g.46704071G>T	NCBI36
NG_008953.1:g.11753G>T , LRG_551:g.11753G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.646G>T MANE Select	ENSP00000308541.5:p.Asp216Tyr
ENST00000311907.9:c.646G>T	ENSP00000308541.5:p.Asp216Tyr
ENST00000442468.1:c.616G>T	ENSP00000387413.1:p.Asp206Tyr
ENST00000490274.1:n.426G>T
ENST00000530231.5:c.646G>T	ENSP00000433907.1:p.Asp216Tyr
NM_000506.3:c.646G>T	NP_000497.1:p.Asp216Tyr
NM_000506.4:c.646G>T , LRG_551t1:c.646G>T	NP_000497.1:p.Asp216Tyr
NM_001311257.1:c.598G>T	NP_001298186.1:p.Asp200Tyr
XR_428840.2:n.690G>T
XR_428840.4:n.681G>T
NM_000506.5:c.646G>T MANE Select	NP_000497.1:p.Asp216Tyr
NM_001311257.2:c.598G>T	NP_001298186.1:p.Asp200Tyr