Canonical Allele Identifier: CA2466846432

Gene: F8

Linked Data

• dbSNP Id: rs2073392137
• gnomAD v4: X-154960956-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154960956A>C , CM000685.2:g.154960956A>C	GRCh38
NC_000023.10:g.154189231A>C , CM000685.1:g.154189231A>C	GRCh37
NC_000023.9:g.153842425A>C	NCBI36
NG_011403.1:g.66768T>G
NG_011403.2:g.66768T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1537+119T>G MANE Select	ENSP00000353393.4:n.1537+119T>G
ENST00000647125.1:c.*1413+119T>G	ENSP00000496062.1:n.*1413+119T>G
ENST00000360256.8:c.1537+119T>G	ENSP00000353393.4:n.1537+119T>G
NM_000132.3:c.1537+119T>G	NP_000123.1:n.1537+119T>G
XM_011531126.1:c.1432+119T>G	XP_011529428.1:n.1432+119T>G
NM_000132.4:c.1537+119T>G MANE Select	NP_000123.1:n.1537+119T>G