Canonical Allele Identifier: CA414908616

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154133145C>A (hg19) ; chrX:g.154904870C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904870C>A , CM000685.2:g.154904870C>A	GRCh38
NC_000023.10:g.154133145C>A , CM000685.1:g.154133145C>A	GRCh37
NC_000023.9:g.153786339C>A	NCBI36
NG_011403.1:g.122854G>T
NG_011403.2:g.122854G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5527G>T MANE Select	ENSP00000353393.4:p.Ala1843Ser
ENST00000360256.8:c.5527G>T	ENSP00000353393.4:p.Ala1843Ser
NM_000132.3:c.5527G>T	NP_000123.1:p.Ala1843Ser
XM_011531126.1:c.5422G>T	XP_011529428.1:p.Ala1808Ser
NM_000132.4:c.5527G>T MANE Select	NP_000123.1:p.Ala1843Ser