Canonical Allele Identifier: CA414905976
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903984A>T , CM000685.2:g.154903984A>T GRCh38
NC_000023.10:g.154132259A>T , CM000685.1:g.154132259A>T GRCh37
NC_000023.9:g.153785453A>T NCBI36
NG_011403.1:g.123740T>A
NG_011403.2:g.123740T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5920T>A MANE Select ENSP00000353393.4:p.Ser1974Thr
ENST00000360256.8:c.5920T>A ENSP00000353393.4:p.Ser1974Thr
NM_000132.3:c.5920T>A NP_000123.1:p.Ser1974Thr
XM_011531126.1:c.5815T>A XP_011529428.1:p.Ser1939Thr
NM_000132.4:c.5920T>A MANE Select NP_000123.1:p.Ser1974Thr