Canonical Allele Identifier: CA2466865487

Gene: F8

Linked Data

• dbSNP Id: rs2073766146

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.155022654_155022660del , CM000685.2:g.155022654_155022660del	GRCh38
NC_000023.10:g.154250929_154250935del , CM000685.1:g.154250929_154250935del	GRCh37
NC_000023.9:g.153904123_153904129del	NCBI36
NG_011403.1:g.5065_5071del
NG_011403.2:g.5065_5071del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.-107_-101del MANE Select	ENSP00000353393.4:n.-107_-101del
ENST00000647125.1:c.-107_-101del	ENSP00000496062.1:n.-107_-101del
ENST00000360256.8:c.-107_-101del	ENSP00000353393.4:n.-107_-101del
ENST00000423959.5:c.38+4121_38+4127del	ENSP00000409446.1:n.38+4121_38+4127del
ENST00000453950.1:c.39-163_39-157del	ENSP00000389153.1:n.39-163_39-157del
NM_000132.3:c.-107_-101del	NP_000123.1:n.-107_-101del
XM_011531126.1:c.38+4121_38+4127del	XP_011529428.1:n.38+4121_38+4127del
NM_000132.4:c.-107_-101del MANE Select	NP_000123.1:n.-107_-101del