Canonical Allele Identifier: CA414918437

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154197815C>A (hg19) ; chrX:g.154969540C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154969540C>A , CM000685.2:g.154969540C>A	GRCh38
NC_000023.10:g.154197815C>A , CM000685.1:g.154197815C>A	GRCh37
NC_000023.9:g.153851009C>A	NCBI36
NG_011403.1:g.58184G>T
NG_011403.2:g.58184G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.800G>T MANE Select	ENSP00000353393.4:p.Cys267Phe
ENST00000647125.1:c.*676G>T	ENSP00000496062.1:n.*676G>T
ENST00000360256.8:c.800G>T	ENSP00000353393.4:p.Cys267Phe
NM_000132.3:c.800G>T	NP_000123.1:p.Cys267Phe
XM_011531126.1:c.695G>T	XP_011529428.1:p.Cys232Phe
NM_000132.4:c.800G>T MANE Select	NP_000123.1:p.Cys267Phe