Canonical Allele Identifier: CA414912817
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154961138A>C , CM000685.2:g.154961138A>C GRCh38
NC_000023.10:g.154189413A>C , CM000685.1:g.154189413A>C GRCh37
NC_000023.9:g.153842607A>C NCBI36
NG_011403.1:g.66586T>G
NG_011403.2:g.66586T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1474T>G MANE Select ENSP00000353393.4:p.Tyr492Asp
ENST00000647125.1:c.*1350T>G ENSP00000496062.1:n.*1350T>G
ENST00000360256.8:c.1474T>G ENSP00000353393.4:p.Tyr492Asp
NM_000132.3:c.1474T>G NP_000123.1:p.Tyr492Asp
XM_011531126.1:c.1369T>G XP_011529428.1:p.Tyr457Asp
NM_000132.4:c.1474T>G MANE Select NP_000123.1:p.Tyr492Asp