Canonical Allele Identifier: CA414897467

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154065984G>T (hg19) ; chrX:g.154837709G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837709G>T , CM000685.2:g.154837709G>T	GRCh38
NC_000023.10:g.154065984G>T , CM000685.1:g.154065984G>T	GRCh37
NC_000023.9:g.153719178G>T	NCBI36
NG_011403.1:g.190015C>A
NG_033065.1:g.1954C>A
NG_011403.2:g.190015C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.6944C>A MANE Select	ENSP00000353393.4:p.Ser2315Tyr
ENST00000644698.1:c.677C>A	ENSP00000495706.1:p.Ser226Tyr
ENST00000330287.10:c.539C>A	ENSP00000327895.6:p.Ser180Tyr
ENST00000360256.8:c.6944C>A	ENSP00000353393.4:p.Ser2315Tyr
NM_000132.3:c.6944C>A	NP_000123.1:p.Ser2315Tyr
NM_019863.2:c.539C>A	NP_063916.1:p.Ser180Tyr
XM_011531126.1:c.6839C>A	XP_011529428.1:p.Ser2280Tyr
NM_000132.4:c.6944C>A MANE Select	NP_000123.1:p.Ser2315Tyr
NM_019863.3:c.539C>A	NP_063916.1:p.Ser180Tyr