Canonical Allele Identifier: CA2824315729

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154961065G>C , CM000685.2:g.154961065G>C	GRCh38
NC_000023.10:g.154189340G>C , CM000685.1:g.154189340G>C	GRCh37
NC_000023.9:g.153842534G>C	NCBI36
NG_011403.1:g.66659C>G
NG_011403.2:g.66659C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1537+10C>G MANE Select	ENSP00000353393.4:n.1537+10C>G
ENST00000647125.1:c.*1413+10C>G	ENSP00000496062.1:n.*1413+10C>G
ENST00000360256.8:c.1537+10C>G	ENSP00000353393.4:n.1537+10C>G
NM_000132.3:c.1537+10C>G	NP_000123.1:n.1537+10C>G
XM_011531126.1:c.1432+10C>G	XP_011529428.1:n.1432+10C>G
NM_000132.4:c.1537+10C>G MANE Select	NP_000123.1:n.1537+10C>G