Canonical Allele Identifier: CA873340712
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 811466
ClinVar RCV Id: RCV001001337
dbSNP Id: rs1216878586

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903989_154903990del , CM000685.2:g.154903989_154903990del GRCh38
NC_000023.10:g.154132264_154132265del , CM000685.1:g.154132264_154132265del GRCh37
NC_000023.9:g.153785458_153785459del NCBI36
NG_011403.1:g.123734_123735del
NG_011403.2:g.123734_123735del

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5914_5915del MANE Select ENSP00000353393.4:p.Ile1972ProfsTer19
ENST00000360256.8:c.5914_5915del ENSP00000353393.4:p.Ile1972ProfsTer19
NM_000132.3:c.5914_5915del NP_000123.1:p.Ile1972ProfsTer19
XM_011531126.1:c.5809_5810del XP_011529428.1:p.Ile1937ProfsTer19
NM_000132.4:c.5914_5915del MANE Select NP_000123.1:p.Ile1972ProfsTer19