Canonical Allele Identifier: CA414896749

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154065906T>A (hg19) ; chrX:g.154837631T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837631T>A , CM000685.2:g.154837631T>A	GRCh38
NC_000023.10:g.154065906T>A , CM000685.1:g.154065906T>A	GRCh37
NC_000023.9:g.153719100T>A	NCBI36
NG_011403.1:g.190093A>T
NG_033065.1:g.2032A>T
NG_011403.2:g.190093A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.7022A>T MANE Select	ENSP00000353393.4:p.Glu2341Val
ENST00000644698.1:c.755A>T	ENSP00000495706.1:p.Glu252Val
ENST00000330287.10:c.617A>T	ENSP00000327895.6:p.Glu206Val
ENST00000360256.8:c.7022A>T	ENSP00000353393.4:p.Glu2341Val
NM_000132.3:c.7022A>T	NP_000123.1:p.Glu2341Val
NM_019863.2:c.617A>T	NP_063916.1:p.Glu206Val
XM_011531126.1:c.6917A>T	XP_011529428.1:p.Glu2306Val
NM_000132.4:c.7022A>T MANE Select	NP_000123.1:p.Glu2341Val
NM_019863.3:c.617A>T	NP_063916.1:p.Glu206Val