Canonical Allele Identifier: CA414914406
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928779G>T , CM000685.2:g.154928779G>T GRCh38
NC_000023.10:g.154157054G>T , CM000685.1:g.154157054G>T GRCh37
NC_000023.9:g.153810248G>T NCBI36
NG_011403.1:g.98945C>A
NG_011403.2:g.98945C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5011C>A MANE Select ENSP00000353393.4:p.Arg1671Ser
ENST00000360256.8:c.5011C>A ENSP00000353393.4:p.Arg1671Ser
NM_000132.3:c.5011C>A NP_000123.1:p.Arg1671Ser
XM_011531126.1:c.4906C>A XP_011529428.1:p.Arg1636Ser
NM_000132.4:c.5011C>A MANE Select NP_000123.1:p.Arg1671Ser