Canonical Allele Identifier: CA414903258

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154088744T>A (hg19) ; chrX:g.154860469T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154860469T>A , CM000685.2:g.154860469T>A	GRCh38
NC_000023.10:g.154088744T>A , CM000685.1:g.154088744T>A	GRCh37
NC_000023.9:g.153741938T>A	NCBI36
NG_011403.1:g.167255A>T
NG_011403.2:g.167255A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6863A>T MANE Select	ENSP00000353393.4:p.His2288Leu
ENST00000644698.1:c.596A>T	ENSP00000495706.1:p.His199Leu
ENST00000330287.10:c.458A>T	ENSP00000327895.6:p.His153Leu
ENST00000360256.8:c.6863A>T	ENSP00000353393.4:p.His2288Leu
NM_000132.3:c.6863A>T	NP_000123.1:p.His2288Leu
NM_019863.2:c.458A>T	NP_063916.1:p.His153Leu
XM_011531126.1:c.6758A>T	XP_011529428.1:p.His2253Leu
NM_000132.4:c.6863A>T MANE Select	NP_000123.1:p.His2288Leu
NM_019863.3:c.458A>T	NP_063916.1:p.His153Leu