Canonical Allele Identifier: CA414906610
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904073A>C , CM000685.2:g.154904073A>C GRCh38
NC_000023.10:g.154132348A>C , CM000685.1:g.154132348A>C GRCh37
NC_000023.9:g.153785542A>C NCBI36
NG_011403.1:g.123651T>G
NG_011403.2:g.123651T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5831T>G MANE Select ENSP00000353393.4:p.Ile1944Arg
ENST00000360256.8:c.5831T>G ENSP00000353393.4:p.Ile1944Arg
NM_000132.3:c.5831T>G NP_000123.1:p.Ile1944Arg
XM_011531126.1:c.5726T>G XP_011529428.1:p.Ile1909Arg
NM_000132.4:c.5831T>G MANE Select NP_000123.1:p.Ile1944Arg