Canonical Allele Identifier: CA2824315513

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154954207G>C , CM000685.2:g.154954207G>C	GRCh38
NC_000023.10:g.154182482G>C , CM000685.1:g.154182482G>C	GRCh37
NC_000023.9:g.153835676G>C	NCBI36
NG_011403.1:g.73517C>G
NG_011403.2:g.73517C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1753-165C>G MANE Select	ENSP00000353393.4:n.1753-165C>G
ENST00000647125.1:c.*1629-165C>G	ENSP00000496062.1:n.*1629-165C>G
ENST00000360256.8:c.1753-165C>G	ENSP00000353393.4:n.1753-165C>G
NM_000132.3:c.1753-165C>G	NP_000123.1:n.1753-165C>G
XM_011531126.1:c.1648-165C>G	XP_011529428.1:n.1648-165C>G
NM_000132.4:c.1753-165C>G MANE Select	NP_000123.1:n.1753-165C>G