Canonical Allele Identifier: CA2579744408

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154896319T>A , CM000685.2:g.154896319T>A	GRCh38
NC_000023.10:g.154124594T>A , CM000685.1:g.154124594T>A	GRCh37
NC_000023.9:g.153777788T>A	NCBI36
NG_011403.1:g.131405A>T
NG_011403.2:g.131405A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6274-87A>T MANE Select	ENSP00000353393.4:n.6274-87A>T
ENST00000360256.8:c.6274-87A>T	ENSP00000353393.4:n.6274-87A>T
NM_000132.3:c.6274-87A>T	NP_000123.1:n.6274-87A>T
XM_011531126.1:c.6169-87A>T	XP_011529428.1:n.6169-87A>T
NM_000132.4:c.6274-87A>T MANE Select	NP_000123.1:n.6274-87A>T