Canonical Allele Identifier: CA2466815659

Gene: F8

Linked Data

• dbSNP Id: rs2072706801

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863168_154863169dup , CM000685.2:g.154863168_154863169dup	GRCh38
NC_000023.10:g.154091443_154091444dup , CM000685.1:g.154091443_154091444dup	GRCh37
NC_000023.9:g.153744637_153744638dup	NCBI36
NG_011403.1:g.164555_164556dup
NG_011403.2:g.164555_164556dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.6488_6489dup MANE Select	ENSP00000353393.4:p.Ile2164LeufsTer23
ENST00000644698.1:c.221_222dup	ENSP00000495706.1:p.Ile75LeufsTer23
ENST00000330287.10:c.83_84dup	ENSP00000327895.6:p.Ile29LeufsTer23
ENST00000360256.8:c.6488_6489dup	ENSP00000353393.4:p.Ile2164LeufsTer23
NM_000132.3:c.6488_6489dup	NP_000123.1:p.Ile2164LeufsTer23
NM_019863.2:c.83_84dup	NP_063916.1:p.Ile29LeufsTer23
XM_011531126.1:c.6383_6384dup	XP_011529428.1:p.Ile2129LeufsTer23
NM_000132.4:c.6488_6489dup MANE Select	NP_000123.1:p.Ile2164LeufsTer23
NM_019863.3:c.83_84dup	NP_063916.1:p.Ile29LeufsTer23