Canonical Allele Identifier: CA10568024

Gene: F8

Linked Data

• dbSNP Id: rs782243113
• ExAC: X:154156804 T / C
• gnomAD v2: X-154156804-T-C
• gnomAD v4: X-154928529-T-C
• MyVariant Identifiers: chrX:g.154156804T>C (hg19) ; chrX:g.154928529T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154928529T>C , CM000685.2:g.154928529T>C	GRCh38
NC_000023.10:g.154156804T>C , CM000685.1:g.154156804T>C	GRCh37
NC_000023.9:g.153809998T>C	NCBI36
NG_011403.1:g.99195A>G
NG_011403.2:g.99195A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.5219+42A>G MANE Select	ENSP00000353393.4:n.5219+42A>G
ENST00000360256.8:c.5219+42A>G	ENSP00000353393.4:n.5219+42A>G
NM_000132.3:c.5219+42A>G	NP_000123.1:n.5219+42A>G
XM_011531126.1:c.5114+42A>G	XP_011529428.1:n.5114+42A>G
NM_000132.4:c.5219+42A>G MANE Select	NP_000123.1:n.5219+42A>G