Canonical Allele Identifier: CA414912879

Gene: F8

Linked Data

• dbSNP Id: rs1557281568
• MyVariant Identifiers: chrX:g.154189428G>A (hg19) ; chrX:g.154961153G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154961153G>A , CM000685.2:g.154961153G>A	GRCh38
NC_000023.10:g.154189428G>A , CM000685.1:g.154189428G>A	GRCh37
NC_000023.9:g.153842622G>A	NCBI36
NG_011403.1:g.66571C>T
NG_011403.2:g.66571C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.1459C>T MANE Select	ENSP00000353393.4:p.Gln487Ter
ENST00000647125.1:c.*1335C>T	ENSP00000496062.1:n.*1335C>T
ENST00000360256.8:c.1459C>T	ENSP00000353393.4:p.Gln487Ter
NM_000132.3:c.1459C>T	NP_000123.1:p.Gln487Ter
XM_011531126.1:c.1354C>T	XP_011529428.1:p.Gln452Ter
NM_000132.4:c.1459C>T MANE Select	NP_000123.1:p.Gln487Ter