Canonical Allele Identifier: CA519718464
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154157097A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928822A>T , CM000685.2:g.154928822A>T GRCh38
NC_000023.10:g.154157097A>T , CM000685.1:g.154157097A>T GRCh37
NC_000023.9:g.153810291A>T NCBI36
NG_011403.1:g.98902T>A
NG_011403.2:g.98902T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.4968T>A MANE Select ENSP00000353393.4:p.Ser1656=
ENST00000360256.8:c.4968T>A ENSP00000353393.4:p.Ser1656=
NM_000132.3:c.4968T>A NP_000123.1:p.Ser1656=
XM_011531126.1:c.4863T>A XP_011529428.1:p.Ser1621=
NM_000132.4:c.4968T>A MANE Select NP_000123.1:p.Ser1656=
Search 100 bp 5'
Search 100 bp 3'