Canonical Allele Identifier: CA255099
Gene: F8 HGNC NCBI

Linked Data

ClinVar Variation Id: 10209
ClinVar RCV Id: RCV000010922
dbSNP Id: rs28933671
MyVariant Identifiers: chrX:g.154194746T>C (hg19) chrX:g.154966471T>C (hg38)
PubMed: PMID:7728145
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154966471T>C , CM000685.2:g.154966471T>C GRCh38
NC_000023.10:g.154194746T>C , CM000685.1:g.154194746T>C GRCh37
NC_000023.9:g.153847940T>C NCBI36
NG_011403.1:g.61253A>G
NG_011403.2:g.61253A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.1226A>G MANE Select ENSP00000353393.4:p.Glu409Gly
ENST00000647125.1:c.*1102A>G ENSP00000496062.1:n.*1102A>G
ENST00000360256.8:c.1226A>G ENSP00000353393.4:p.Glu409Gly
ENST00000483822.2:n.46A>G
NM_000132.3:c.1226A>G NP_000123.1:p.Glu409Gly
XM_011531126.1:c.1121A>G XP_011529428.1:p.Glu374Gly
NM_000132.4:c.1226A>G MANE Select NP_000123.1:p.Glu409Gly
Search 100 bp 5'
Search 100 bp 3'