Canonical Allele Identifier: CA414905887
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903973G>C , CM000685.2:g.154903973G>C GRCh38
NC_000023.10:g.154132248G>C , CM000685.1:g.154132248G>C GRCh37
NC_000023.9:g.153785442G>C NCBI36
NG_011403.1:g.123751C>G
NG_011403.2:g.123751C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5931C>G MANE Select ENSP00000353393.4:p.Phe1977Leu
ENST00000360256.8:c.5931C>G ENSP00000353393.4:p.Phe1977Leu
NM_000132.3:c.5931C>G NP_000123.1:p.Phe1977Leu
XM_011531126.1:c.5826C>G XP_011529428.1:p.Phe1942Leu
NM_000132.4:c.5931C>G MANE Select NP_000123.1:p.Phe1977Leu