Canonical Allele Identifier: CA873357403

Gene: F8

Linked Data

• dbSNP Id: rs1438599611
• gnomAD v3: X-154996883-A-C
• gnomAD v4: X-154996883-A-C
• MyVariant Identifiers: chrX:g.154996883A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154996883A>C , CM000685.2:g.154996883A>C	GRCh38
NC_000023.10:g.154225158A>C , CM000685.1:g.154225158A>C	GRCh37
NC_000023.9:g.153878352A>C	NCBI36
NG_011403.1:g.30841T>G
NG_011403.2:g.30841T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.388+90T>G MANE Select	ENSP00000353393.4:n.388+90T>G
ENST00000647125.1:c.*174+90T>G	ENSP00000496062.1:n.*174+90T>G
ENST00000360256.8:c.388+90T>G	ENSP00000353393.4:n.388+90T>G
ENST00000423959.5:c.283+90T>G	ENSP00000409446.1:n.283+90T>G
ENST00000453950.1:c.370+90T>G	ENSP00000389153.1:n.370+90T>G
NM_000132.3:c.388+90T>G	NP_000123.1:n.388+90T>G
XM_011531126.1:c.283+90T>G	XP_011529428.1:n.283+90T>G
NM_000132.4:c.388+90T>G MANE Select	NP_000123.1:n.388+90T>G