Canonical Allele Identifier: CA915952191

Gene: F8

Linked Data

• ClinVar Variation Id: 627137
• ClinVar RCV Id: RCV000851881
• dbSNP Id: rs1603435417

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154969566A>C , CM000685.2:g.154969566A>C	GRCh38
NC_000023.10:g.154197841A>C , CM000685.1:g.154197841A>C	GRCh37
NC_000023.9:g.153851035A>C	NCBI36
NG_011403.1:g.58158T>G
NG_011403.2:g.58158T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.788-14T>G MANE Select	ENSP00000353393.4:n.788-14T>G
ENST00000647125.1:c.*664-14T>G	ENSP00000496062.1:n.*664-14T>G
ENST00000360256.8:c.788-14T>G	ENSP00000353393.4:n.788-14T>G
NM_000132.3:c.788-14T>G	NP_000123.1:n.788-14T>G
XM_011531126.1:c.683-14T>G	XP_011529428.1:n.683-14T>G
NM_000132.4:c.788-14T>G MANE Select	NP_000123.1:n.788-14T>G