Canonical Allele Identifier: CA414909163
Gene: F8 HGNC NCBI

Linked Data

COSMIC: COSM5716659 COSM5716660
MyVariant Identifiers: chrX:g.154133294G>A (hg19) chrX:g.154905019G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154905019G>A , CM000685.2:g.154905019G>A GRCh38
NC_000023.10:g.154133294G>A , CM000685.1:g.154133294G>A GRCh37
NC_000023.9:g.153786488G>A NCBI36
NG_011403.1:g.122705C>T
NG_011403.2:g.122705C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5378C>T MANE Select ENSP00000353393.4:p.Thr1793Ile
ENST00000360256.8:c.5378C>T ENSP00000353393.4:p.Thr1793Ile
NM_000132.3:c.5378C>T NP_000123.1:p.Thr1793Ile
XM_011531126.1:c.5273C>T XP_011529428.1:p.Thr1758Ile
NM_000132.4:c.5378C>T MANE Select NP_000123.1:p.Thr1793Ile
Search 100 bp 5'
Search 100 bp 3'