Canonical Allele Identifier: CA5967012

Gene: F2

Linked Data

• dbSNP Id: rs764778271
• ExAC: 11:46747414 G / T
• gnomAD v2: 11-46747414-G-T
• gnomAD v4: 11-46725864-G-T
• MyVariant Identifiers: chr11:g.46747414G>T (hg19) ; chr11:g.46725864G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725864G>T , CM000673.2:g.46725864G>T	GRCh38
NC_000011.9:g.46747414G>T , CM000673.1:g.46747414G>T	GRCh37
NC_000011.8:g.46703990G>T	NCBI36
NG_008953.1:g.11672G>T , LRG_551:g.11672G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.565G>T MANE Select	ENSP00000308541.5:p.Asp189Tyr
ENST00000311907.9:c.565G>T	ENSP00000308541.5:p.Asp189Tyr
ENST00000442468.1:c.535G>T	ENSP00000387413.1:p.Asp179Tyr
ENST00000490274.1:n.345G>T
ENST00000530231.5:c.565G>T	ENSP00000433907.1:p.Asp189Tyr
NM_000506.3:c.565G>T	NP_000497.1:p.Asp189Tyr
NM_000506.4:c.565G>T , LRG_551t1:c.565G>T	NP_000497.1:p.Asp189Tyr
NM_001311257.1:c.517G>T	NP_001298186.1:p.Asp173Tyr
XR_428840.2:n.609G>T
XR_428840.4:n.600G>T
NM_000506.5:c.565G>T MANE Select	NP_000497.1:p.Asp189Tyr
NM_001311257.2:c.517G>T	NP_001298186.1:p.Asp173Tyr