Canonical Allele Identifier: CA873341388
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1342455699
MyVariant Identifiers: chrX:g.154905015_154905016insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154905018dup , CM000685.2:g.154905018dup GRCh38
NC_000023.10:g.154133293dup , CM000685.1:g.154133293dup GRCh37
NC_000023.9:g.153786487dup NCBI36
NG_011403.1:g.122708dup
NG_011403.2:g.122708dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5381dup MANE Select ENSP00000353393.4:p.Arg1795GlnfsTer13
ENST00000360256.8:c.5381dup ENSP00000353393.4:p.Arg1795GlnfsTer13
NM_000132.3:c.5381dup NP_000123.1:p.Arg1795GlnfsTer13
XM_011531126.1:c.5276dup XP_011529428.1:p.Arg1760GlnfsTer13
NM_000132.4:c.5381dup MANE Select NP_000123.1:p.Arg1795GlnfsTer13
Search 100 bp 5'
Search 100 bp 3'