Canonical Allele Identifier: CA2466828513

Gene: F8

Linked Data

• dbSNP Id: rs2073031635

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154905086_154905087dup , CM000685.2:g.154905086_154905087dup	GRCh38
NC_000023.10:g.154133361_154133362dup , CM000685.1:g.154133361_154133362dup	GRCh37
NC_000023.9:g.153786555_153786556dup	NCBI36
NG_011403.1:g.122637_122638dup
NG_011403.2:g.122637_122638dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5374-64_5374-63dup MANE Select	ENSP00000353393.4:n.5374-64_5374-63dup
ENST00000360256.8:c.5374-64_5374-63dup	ENSP00000353393.4:n.5374-64_5374-63dup
NM_000132.3:c.5374-64_5374-63dup	NP_000123.1:n.5374-64_5374-63dup
XM_011531126.1:c.5269-64_5269-63dup	XP_011529428.1:n.5269-64_5269-63dup
NM_000132.4:c.5374-64_5374-63dup MANE Select	NP_000123.1:n.5374-64_5374-63dup