Canonical Allele Identifier: CA519384102
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154225270T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154996995T>A , CM000685.2:g.154996995T>A GRCh38
NC_000023.10:g.154225270T>A , CM000685.1:g.154225270T>A GRCh37
NC_000023.9:g.153878464T>A NCBI36
NG_011403.1:g.30729A>T
NG_011403.2:g.30729A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.366A>T MANE Select ENSP00000353393.4:p.Val122=
ENST00000647125.1:c.*152A>T ENSP00000496062.1:n.*152A>T
ENST00000360256.8:c.366A>T ENSP00000353393.4:p.Val122=
ENST00000423959.5:c.261A>T ENSP00000409446.1:p.Val87=
ENST00000453950.1:c.348A>T ENSP00000389153.1:p.Val116=
NM_000132.3:c.366A>T NP_000123.1:p.Val122=
XM_011531126.1:c.261A>T XP_011529428.1:p.Val87=
NM_000132.4:c.366A>T MANE Select NP_000123.1:p.Val122=