Canonical Allele Identifier: CA873341329

Gene: F8

Linked Data

• dbSNP Id: rs1216722366
• MyVariant Identifiers: chrX:g.154904891del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904894del , CM000685.2:g.154904894del	GRCh38
NC_000023.10:g.154133169del , CM000685.1:g.154133169del	GRCh37
NC_000023.9:g.153786363del	NCBI36
NG_011403.1:g.122833del
NG_011403.2:g.122833del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5506del MANE Select	ENSP00000353393.4:p.Trp1836GlyfsTer?
ENST00000360256.8:c.5506del	ENSP00000353393.4:p.Trp1836GlyfsTer?
NM_000132.3:c.5506del	NP_000123.1:p.Trp1836GlyfsTer?
XM_011531126.1:c.5401del	XP_011529428.1:p.Trp1801GlyfsTer?
NM_000132.4:c.5506del MANE Select	NP_000123.1:p.Trp1836GlyfsTer?