Canonical Allele Identifier: CA519367140

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154197643C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154969368C>T , CM000685.2:g.154969368C>T	GRCh38
NC_000023.10:g.154197643C>T , CM000685.1:g.154197643C>T	GRCh37
NC_000023.9:g.153850837C>T	NCBI36
NG_011403.1:g.58356G>A
NG_011403.2:g.58356G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.972G>A MANE Select	ENSP00000353393.4:p.Gln324=
ENST00000647125.1:c.*848G>A	ENSP00000496062.1:n.*848G>A
ENST00000360256.8:c.972G>A	ENSP00000353393.4:p.Gln324=
NM_000132.3:c.972G>A	NP_000123.1:p.Gln324=
XM_011531126.1:c.867G>A	XP_011529428.1:p.Gln289=
NM_000132.4:c.972G>A MANE Select	NP_000123.1:p.Gln324=