Canonical Allele Identifier: CA873354159

Gene: F8

Linked Data

• dbSNP Id: rs1328186809
• gnomAD v3: X-154957358-G-GT
• gnomAD v4: X-154957358-G-GT
• MyVariant Identifiers: chrX:g.154957358_154957359insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154957359dup , CM000685.2:g.154957359dup	GRCh38
NC_000023.10:g.154185634dup , CM000685.1:g.154185634dup	GRCh37
NC_000023.9:g.153838828dup	NCBI36
NG_011403.1:g.70365dup
NG_011403.2:g.70365dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1538-188dup MANE Select	ENSP00000353393.4:n.1538-188dup
ENST00000647125.1:c.*1414-188dup	ENSP00000496062.1:n.*1414-188dup
ENST00000360256.8:c.1538-188dup	ENSP00000353393.4:n.1538-188dup
NM_000132.3:c.1538-188dup	NP_000123.1:n.1538-188dup
XM_011531126.1:c.1433-188dup	XP_011529428.1:n.1433-188dup
NM_000132.4:c.1538-188dup MANE Select	NP_000123.1:n.1538-188dup