Canonical Allele Identifier: CA2527868749

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904639A>G , CM000685.2:g.154904639A>G	GRCh38
NC_000023.10:g.154132914A>G , CM000685.1:g.154132914A>G	GRCh37
NC_000023.9:g.153786108A>G	NCBI36
NG_011403.1:g.123085T>C
NG_011403.2:g.123085T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5587-115T>C MANE Select	ENSP00000353393.4:n.5587-115T>C
ENST00000360256.8:c.5587-115T>C	ENSP00000353393.4:n.5587-115T>C
NM_000132.3:c.5587-115T>C	NP_000123.1:n.5587-115T>C
XM_011531126.1:c.5482-115T>C	XP_011529428.1:n.5482-115T>C
NM_000132.4:c.5587-115T>C MANE Select	NP_000123.1:n.5587-115T>C