Canonical Allele Identifier: CA414907326

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154091412G>A (hg19) ; chrX:g.154863137G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863137G>A , CM000685.2:g.154863137G>A	GRCh38
NC_000023.10:g.154091412G>A , CM000685.1:g.154091412G>A	GRCh37
NC_000023.9:g.153744606G>A	NCBI36
NG_011403.1:g.164587C>T
NG_011403.2:g.164587C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.6520C>T MANE Select	ENSP00000353393.4:p.His2174Tyr
ENST00000644698.1:c.253C>T	ENSP00000495706.1:p.His85Tyr
ENST00000330287.10:c.115C>T	ENSP00000327895.6:p.His39Tyr
ENST00000360256.8:c.6520C>T	ENSP00000353393.4:p.His2174Tyr
NM_000132.3:c.6520C>T	NP_000123.1:p.His2174Tyr
NM_019863.2:c.115C>T	NP_063916.1:p.His39Tyr
XM_011531126.1:c.6415C>T	XP_011529428.1:p.His2139Tyr
NM_000132.4:c.6520C>T MANE Select	NP_000123.1:p.His2174Tyr
NM_019863.3:c.115C>T	NP_063916.1:p.His39Tyr