Canonical Allele Identifier: CA519355850
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1557275987
gnomAD v2: X-154130363-A-G
gnomAD v4: X-154902088-A-G
MyVariant Identifiers: chrX:g.154130363A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154902088A>G , CM000685.2:g.154902088A>G GRCh38
NC_000023.10:g.154130363A>G , CM000685.1:g.154130363A>G GRCh37
NC_000023.9:g.153783557A>G NCBI36
NG_011403.1:g.125636T>C
NG_011403.2:g.125636T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6078T>C MANE Select ENSP00000353393.4:p.His2026=
ENST00000360256.8:c.6078T>C ENSP00000353393.4:p.His2026=
NM_000132.3:c.6078T>C NP_000123.1:p.His2026=
XM_011531126.1:c.5973T>C XP_011529428.1:p.His1991=
NM_000132.4:c.6078T>C MANE Select NP_000123.1:p.His2026=
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