Canonical Allele Identifier: CA2466828169

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904018A= , CM000685.2:g.154904018A=	GRCh38
NC_000023.10:g.154132293A= , CM000685.1:g.154132293A=	GRCh37
NC_000023.9:g.153785487A=	NCBI36
NG_011403.1:g.123706T=
NG_011403.2:g.123706T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.5886T= MANE Select	ENSP00000353393.4:p.Tyr1962=
ENST00000360256.8:c.5886T=	ENSP00000353393.4:p.Tyr1962=
NM_000132.3:c.5886T=	NP_000123.1:p.Tyr1962=
XM_011531126.1:c.5781T=	XP_011529428.1:p.Tyr1927=
NM_000132.4:c.5886T= MANE Select	NP_000123.1:p.Tyr1962=