Canonical Allele Identifier: CA2695237915

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154903903T>G , CM000685.2:g.154903903T>G	GRCh38
NC_000023.10:g.154132178T>G , CM000685.1:g.154132178T>G	GRCh37
NC_000023.9:g.153785372T>G	NCBI36
NG_011403.1:g.123821A>C
NG_011403.2:g.123821A>C

Transcript Alleles

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