Canonical Allele Identifier: CA2466835692

Gene: F8

Linked Data

• dbSNP Id: rs2073171549

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154928445T>G , CM000685.2:g.154928445T>G	GRCh38
NC_000023.10:g.154156720T>G , CM000685.1:g.154156720T>G	GRCh37
NC_000023.9:g.153809914T>G	NCBI36
NG_011403.1:g.99279A>C
NG_011403.2:g.99279A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.5219+126A>C MANE Select	ENSP00000353393.4:n.5219+126A>C
ENST00000360256.8:c.5219+126A>C	ENSP00000353393.4:n.5219+126A>C
NM_000132.3:c.5219+126A>C	NP_000123.1:n.5219+126A>C
XM_011531126.1:c.5114+126A>C	XP_011529428.1:n.5114+126A>C
NM_000132.4:c.5219+126A>C MANE Select	NP_000123.1:n.5219+126A>C