Canonical Allele Identifier: CA2466828029

Gene: F8

Linked Data

• dbSNP Id: rs2073020753

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154903545G>C , CM000685.2:g.154903545G>C	GRCh38
NC_000023.10:g.154131820G>C , CM000685.1:g.154131820G>C	GRCh37
NC_000023.9:g.153785014G>C	NCBI36
NG_011403.1:g.124179C>G
NG_011403.2:g.124179C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5998+361C>G MANE Select	ENSP00000353393.4:n.5998+361C>G
ENST00000360256.8:c.5998+361C>G	ENSP00000353393.4:n.5998+361C>G
NM_000132.3:c.5998+361C>G	NP_000123.1:n.5998+361C>G
XM_011531126.1:c.5893+361C>G	XP_011529428.1:n.5893+361C>G
NM_000132.4:c.5998+361C>G MANE Select	NP_000123.1:n.5998+361C>G