Canonical Allele Identifier: CA414911963

Gene: F8

Linked Data

• gnomAD v4: X-154957096-T-A
• MyVariant Identifiers: chrX:g.154185371T>A (hg19) ; chrX:g.154957096T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154957096T>A , CM000685.2:g.154957096T>A	GRCh38
NC_000023.10:g.154185371T>A , CM000685.1:g.154185371T>A	GRCh37
NC_000023.9:g.153838565T>A	NCBI36
NG_011403.1:g.70628A>T
NG_011403.2:g.70628A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1613A>T MANE Select	ENSP00000353393.4:p.Asp538Val
ENST00000647125.1:c.*1489A>T	ENSP00000496062.1:n.*1489A>T
ENST00000360256.8:c.1613A>T	ENSP00000353393.4:p.Asp538Val
NM_000132.3:c.1613A>T	NP_000123.1:p.Asp538Val
XM_011531126.1:c.1508A>T	XP_011529428.1:p.Asp503Val
NM_000132.4:c.1613A>T MANE Select	NP_000123.1:p.Asp538Val