Canonical Allele Identifier: CA2466846442

Gene: F8

Linked Data

• dbSNP Id: rs2073392332

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154960970C>G , CM000685.2:g.154960970C>G	GRCh38
NC_000023.10:g.154189245C>G , CM000685.1:g.154189245C>G	GRCh37
NC_000023.9:g.153842439C>G	NCBI36
NG_011403.1:g.66754G>C
NG_011403.2:g.66754G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1537+105G>C MANE Select	ENSP00000353393.4:n.1537+105G>C
ENST00000647125.1:c.*1413+105G>C	ENSP00000496062.1:n.*1413+105G>C
ENST00000360256.8:c.1537+105G>C	ENSP00000353393.4:n.1537+105G>C
NM_000132.3:c.1537+105G>C	NP_000123.1:n.1537+105G>C
XM_011531126.1:c.1432+105G>C	XP_011529428.1:n.1432+105G>C
NM_000132.4:c.1537+105G>C MANE Select	NP_000123.1:n.1537+105G>C