Canonical Allele Identifier: CA2466815579

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863099C= , CM000685.2:g.154863099C=	GRCh38
NC_000023.10:g.154091374C= , CM000685.1:g.154091374C=	GRCh37
NC_000023.9:g.153744568C=	NCBI36
NG_011403.1:g.164625G=
NG_011403.2:g.164625G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6558G= MANE Select	ENSP00000353393.4:p.Met2186=
ENST00000644698.1:c.291G=	ENSP00000495706.1:p.Met97=
ENST00000330287.10:c.153G=	ENSP00000327895.6:p.Met51=
ENST00000360256.8:c.6558G=	ENSP00000353393.4:p.Met2186=
NM_000132.3:c.6558G=	NP_000123.1:p.Met2186=
NM_019863.2:c.153G=	NP_063916.1:p.Met51=
XM_011531126.1:c.6453G=	XP_011529428.1:p.Met2151=
NM_000132.4:c.6558G= MANE Select	NP_000123.1:p.Met2186=
NM_019863.3:c.153G=	NP_063916.1:p.Met51=