Canonical Allele Identifier: CA519356097

Gene: F8

Linked Data

• gnomAD v4: X-154903922-C-T
• MyVariant Identifiers: chrX:g.154132197C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154903922C>T , CM000685.2:g.154903922C>T	GRCh38
NC_000023.10:g.154132197C>T , CM000685.1:g.154132197C>T	GRCh37
NC_000023.9:g.153785391C>T	NCBI36
NG_011403.1:g.123802G>A
NG_011403.2:g.123802G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5982G>A MANE Select	ENSP00000353393.4:p.Leu1994=
ENST00000360256.8:c.5982G>A	ENSP00000353393.4:p.Leu1994=
NM_000132.3:c.5982G>A	NP_000123.1:p.Leu1994=
XM_011531126.1:c.5877G>A	XP_011529428.1:p.Leu1959=
NM_000132.4:c.5982G>A MANE Select	NP_000123.1:p.Leu1994=