Canonical Allele Identifier: CA519384178
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154225368G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997093G>A , CM000685.2:g.154997093G>A GRCh38
NC_000023.10:g.154225368G>A , CM000685.1:g.154225368G>A GRCh37
NC_000023.9:g.153878562G>A NCBI36
NG_011403.1:g.30631C>T
NG_011403.2:g.30631C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.268C>T MANE Select ENSP00000353393.4:p.Leu90=
ENST00000647125.1:c.*54C>T ENSP00000496062.1:n.*54C>T
ENST00000360256.8:c.268C>T ENSP00000353393.4:p.Leu90=
ENST00000423959.5:c.163C>T ENSP00000409446.1:p.Leu55=
ENST00000453950.1:c.250C>T ENSP00000389153.1:p.Leu84=
NM_000132.3:c.268C>T NP_000123.1:p.Leu90=
XM_011531126.1:c.163C>T XP_011529428.1:p.Leu55=
NM_000132.4:c.268C>T MANE Select NP_000123.1:p.Leu90=