Canonical Allele Identifier: CA1138601561

Gene: F8

Linked Data

• dbSNP Id: rs2073370757
• gnomAD v3: X-154957410-A-AGAGCTTG
• gnomAD v4: X-154957410-A-AGAGCTTG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154957412_154957418dup , CM000685.2:g.154957412_154957418dup	GRCh38
NC_000023.10:g.154185687_154185693dup , CM000685.1:g.154185687_154185693dup	GRCh37
NC_000023.9:g.153838881_153838887dup	NCBI36
NG_011403.1:g.70307_70313dup
NG_011403.2:g.70307_70313dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1538-246_1538-240dup MANE Select	ENSP00000353393.4:n.1538-246_1538-240dup
ENST00000647125.1:c.*1414-246_*1414-240dup	ENSP00000496062.1:n.*1414-246_*1414-240dup
ENST00000360256.8:c.1538-246_1538-240dup	ENSP00000353393.4:n.1538-246_1538-240dup
NM_000132.3:c.1538-246_1538-240dup	NP_000123.1:n.1538-246_1538-240dup
XM_011531126.1:c.1433-246_1433-240dup	XP_011529428.1:n.1433-246_1433-240dup
NM_000132.4:c.1538-246_1538-240dup MANE Select	NP_000123.1:n.1538-246_1538-240dup