Canonical Allele Identifier: CA380264788

Gene: F2

Linked Data

• MyVariant Identifiers: chr11:g.46747464T>G (hg19) ; chr11:g.46725914T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46725914T>G , CM000673.2:g.46725914T>G	GRCh38
NC_000011.9:g.46747464T>G , CM000673.1:g.46747464T>G	GRCh37
NC_000011.8:g.46704040T>G	NCBI36
NG_008953.1:g.11722T>G , LRG_551:g.11722T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000311907.10:c.615T>G MANE Select	ENSP00000308541.5:p.Asn205Lys
ENST00000311907.9:c.615T>G	ENSP00000308541.5:p.Asn205Lys
ENST00000442468.1:c.585T>G	ENSP00000387413.1:p.Asn195Lys
ENST00000490274.1:n.395T>G
ENST00000530231.5:c.615T>G	ENSP00000433907.1:p.Asn205Lys
NM_000506.3:c.615T>G	NP_000497.1:p.Asn205Lys
NM_000506.4:c.615T>G , LRG_551t1:c.615T>G	NP_000497.1:p.Asn205Lys
NM_001311257.1:c.567T>G	NP_001298186.1:p.Asn189Lys
XR_428840.2:n.659T>G
XR_428840.4:n.650T>G
NM_000506.5:c.615T>G MANE Select	NP_000497.1:p.Asn205Lys
NM_001311257.2:c.567T>G	NP_001298186.1:p.Asn189Lys