Canonical Allele Identifier: CA414913638

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154156896C>A (hg19) ; chrX:g.154928621C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154928621C>A , CM000685.2:g.154928621C>A	GRCh38
NC_000023.10:g.154156896C>A , CM000685.1:g.154156896C>A	GRCh37
NC_000023.9:g.153810090C>A	NCBI36
NG_011403.1:g.99103G>T
NG_011403.2:g.99103G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5169G>T MANE Select	ENSP00000353393.4:p.Glu1723Asp
ENST00000360256.8:c.5169G>T	ENSP00000353393.4:p.Glu1723Asp
NM_000132.3:c.5169G>T	NP_000123.1:p.Glu1723Asp
XM_011531126.1:c.5064G>T	XP_011529428.1:p.Glu1688Asp
NM_000132.4:c.5169G>T MANE Select	NP_000123.1:p.Glu1723Asp