Canonical Allele Identifier: CA414897817

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154066015T>A (hg19) ; chrX:g.154837740T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837740T>A , CM000685.2:g.154837740T>A	GRCh38
NC_000023.10:g.154066015T>A , CM000685.1:g.154066015T>A	GRCh37
NC_000023.9:g.153719209T>A	NCBI36
NG_011403.1:g.189984A>T
NG_033065.1:g.1923A>T
NG_011403.2:g.189984A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6913A>T MANE Select	ENSP00000353393.4:p.Asn2305Tyr
ENST00000644698.1:c.646A>T	ENSP00000495706.1:p.Asn216Tyr
ENST00000330287.10:c.508A>T	ENSP00000327895.6:p.Asn170Tyr
ENST00000360256.8:c.6913A>T	ENSP00000353393.4:p.Asn2305Tyr
NM_000132.3:c.6913A>T	NP_000123.1:p.Asn2305Tyr
NM_019863.2:c.508A>T	NP_063916.1:p.Asn170Tyr
XM_011531126.1:c.6808A>T	XP_011529428.1:p.Asn2270Tyr
NM_000132.4:c.6913A>T MANE Select	NP_000123.1:p.Asn2305Tyr
NM_019863.3:c.508A>T	NP_063916.1:p.Asn170Tyr