Canonical Allele Identifier: CA873353663

Gene: F8

Linked Data

• dbSNP Id: rs1341504858
• MyVariant Identifiers: chrX:g.154956902_154956903insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154956903dup , CM000685.2:g.154956903dup	GRCh38
NC_000023.10:g.154185178dup , CM000685.1:g.154185178dup	GRCh37
NC_000023.9:g.153838372dup	NCBI36
NG_011403.1:g.70821dup
NG_011403.2:g.70821dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.1752+54dup MANE Select	ENSP00000353393.4:n.1752+54dup
ENST00000647125.1:c.*1628+54dup	ENSP00000496062.1:n.*1628+54dup
ENST00000360256.8:c.1752+54dup	ENSP00000353393.4:n.1752+54dup
NM_000132.3:c.1752+54dup	NP_000123.1:n.1752+54dup
XM_011531126.1:c.1647+54dup	XP_011529428.1:n.1647+54dup
NM_000132.4:c.1752+54dup MANE Select	NP_000123.1:n.1752+54dup