Canonical Allele Identifier: CA414906071

Gene: F8

Linked Data

• gnomAD v4: X-154904000-G-T
• MyVariant Identifiers: chrX:g.154132275G>T (hg19) ; chrX:g.154904000G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904000G>T , CM000685.2:g.154904000G>T	GRCh38
NC_000023.10:g.154132275G>T , CM000685.1:g.154132275G>T	GRCh37
NC_000023.9:g.153785469G>T	NCBI36
NG_011403.1:g.123724C>A
NG_011403.2:g.123724C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5904C>A MANE Select	ENSP00000353393.4:p.Ser1968Arg
ENST00000360256.8:c.5904C>A	ENSP00000353393.4:p.Ser1968Arg
NM_000132.3:c.5904C>A	NP_000123.1:p.Ser1968Arg
XM_011531126.1:c.5799C>A	XP_011529428.1:p.Ser1933Arg
NM_000132.4:c.5904C>A MANE Select	NP_000123.1:p.Ser1968Arg