Canonical Allele Identifier: CA414909167
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs2073030896

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154905019G>T , CM000685.2:g.154905019G>T GRCh38
NC_000023.10:g.154133294G>T , CM000685.1:g.154133294G>T GRCh37
NC_000023.9:g.153786488G>T NCBI36
NG_011403.1:g.122705C>A
NG_011403.2:g.122705C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5378C>A MANE Select ENSP00000353393.4:p.Thr1793Asn
ENST00000360256.8:c.5378C>A ENSP00000353393.4:p.Thr1793Asn
NM_000132.3:c.5378C>A NP_000123.1:p.Thr1793Asn
XM_011531126.1:c.5273C>A XP_011529428.1:p.Thr1758Asn
NM_000132.4:c.5378C>A MANE Select NP_000123.1:p.Thr1793Asn