Canonical Allele Identifier: CA873340036
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1436490729
gnomAD v3: X-154928488-TCTAA-T
gnomAD v4: X-154928488-TCTAA-T
MyVariant Identifiers: chrX:g.154928489_154928492del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928491_154928494del , CM000685.2:g.154928491_154928494del GRCh38
NC_000023.10:g.154156766_154156769del , CM000685.1:g.154156766_154156769del GRCh37
NC_000023.9:g.153809960_153809963del NCBI36
NG_011403.1:g.99232_99235del
NG_011403.2:g.99232_99235del

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5219+79_5219+82del MANE Select ENSP00000353393.4:n.5219+79_5219+82del
ENST00000360256.8:c.5219+79_5219+82del ENSP00000353393.4:n.5219+79_5219+82del
NM_000132.3:c.5219+79_5219+82del NP_000123.1:n.5219+79_5219+82del
XM_011531126.1:c.5114+79_5114+82del XP_011529428.1:n.5114+79_5114+82del
NM_000132.4:c.5219+79_5219+82del MANE Select NP_000123.1:n.5219+79_5219+82del
Search 100 bp 5'
Search 100 bp 3'