Canonical Allele Identifier: CA414913506

Gene: F8

Linked Data

• gnomAD v4: X-154928592-G-T
• MyVariant Identifiers: chrX:g.154156867G>T (hg19) ; chrX:g.154928592G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154928592G>T , CM000685.2:g.154928592G>T	GRCh38
NC_000023.10:g.154156867G>T , CM000685.1:g.154156867G>T	GRCh37
NC_000023.9:g.153810061G>T	NCBI36
NG_011403.1:g.99132C>A
NG_011403.2:g.99132C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.5198C>A MANE Select	ENSP00000353393.4:p.Ser1733Tyr
ENST00000360256.8:c.5198C>A	ENSP00000353393.4:p.Ser1733Tyr
NM_000132.3:c.5198C>A	NP_000123.1:p.Ser1733Tyr
XM_011531126.1:c.5093C>A	XP_011529428.1:p.Ser1698Tyr
NM_000132.4:c.5198C>A MANE Select	NP_000123.1:p.Ser1733Tyr