Canonical Allele Identifier: CA2466842818
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs2073320588
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154948713C>G , CM000685.2:g.154948713C>G GRCh38
NC_000023.10:g.154176988C>G , CM000685.1:g.154176988C>G GRCh37
NC_000023.9:g.153830182C>G NCBI36
NG_011403.1:g.79011G>C
NG_011403.2:g.79011G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.1904-806G>C MANE Select ENSP00000353393.4:n.1904-806G>C
ENST00000647125.1:c.*1779+5179G>C ENSP00000496062.1:n.*1779+5179G>C
ENST00000360256.8:c.1904-806G>C ENSP00000353393.4:n.1904-806G>C
NM_000132.3:c.1904-806G>C NP_000123.1:n.1904-806G>C
XM_011531126.1:c.1799-806G>C XP_011529428.1:n.1799-806G>C
NM_000132.4:c.1904-806G>C MANE Select NP_000123.1:n.1904-806G>C
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