Canonical Allele Identifier: CA519384157
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154225345A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997070A>T , CM000685.2:g.154997070A>T GRCh38
NC_000023.10:g.154225345A>T , CM000685.1:g.154225345A>T GRCh37
NC_000023.9:g.153878539A>T NCBI36
NG_011403.1:g.30654T>A
NG_011403.2:g.30654T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.291T>A MANE Select ENSP00000353393.4:p.Ala97=
ENST00000647125.1:c.*77T>A ENSP00000496062.1:n.*77T>A
ENST00000360256.8:c.291T>A ENSP00000353393.4:p.Ala97=
ENST00000423959.5:c.186T>A ENSP00000409446.1:p.Ala62=
ENST00000453950.1:c.273T>A ENSP00000389153.1:p.Ala91=
NM_000132.3:c.291T>A NP_000123.1:p.Ala97=
XM_011531126.1:c.186T>A XP_011529428.1:p.Ala62=
NM_000132.4:c.291T>A MANE Select NP_000123.1:p.Ala97=
Search 100 bp 5'
Search 100 bp 3'