Canonical Allele Identifier: CA873338115

Gene: F8

Linked Data

• dbSNP Id: rs1166136504
• gnomAD v3: X-154896356-T-C
• gnomAD v4: X-154896356-T-C
• MyVariant Identifiers: chrX:g.154896356T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154896356T>C , CM000685.2:g.154896356T>C	GRCh38
NC_000023.10:g.154124631T>C , CM000685.1:g.154124631T>C	GRCh37
NC_000023.9:g.153777825T>C	NCBI36
NG_011403.1:g.131368A>G
NG_011403.2:g.131368A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6274-124A>G MANE Select	ENSP00000353393.4:n.6274-124A>G
ENST00000360256.8:c.6274-124A>G	ENSP00000353393.4:n.6274-124A>G
NM_000132.3:c.6274-124A>G	NP_000123.1:n.6274-124A>G
XM_011531126.1:c.6169-124A>G	XP_011529428.1:n.6169-124A>G
NM_000132.4:c.6274-124A>G MANE Select	NP_000123.1:n.6274-124A>G