Canonical Allele Identifier: CA2466827621

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154902055G= , CM000685.2:g.154902055G=	GRCh38
NC_000023.10:g.154130330G= , CM000685.1:g.154130330G=	GRCh37
NC_000023.9:g.153783524G=	NCBI36
NG_011403.1:g.125669C=
NG_011403.2:g.125669C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.6111C= MANE Select	ENSP00000353393.4:p.Ser2037=
ENST00000360256.8:c.6111C=	ENSP00000353393.4:p.Ser2037=
NM_000132.3:c.6111C=	NP_000123.1:p.Ser2037=
XM_011531126.1:c.6006C=	XP_011529428.1:p.Ser2002=
NM_000132.4:c.6111C= MANE Select	NP_000123.1:p.Ser2037=