Canonical Allele Identifier: CA414905654
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903942C>T , CM000685.2:g.154903942C>T GRCh38
NC_000023.10:g.154132217C>T , CM000685.1:g.154132217C>T GRCh37
NC_000023.9:g.153785411C>T NCBI36
NG_011403.1:g.123782G>A
NG_011403.2:g.123782G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5962G>A MANE Select ENSP00000353393.4:p.Glu1988Lys
ENST00000360256.8:c.5962G>A ENSP00000353393.4:p.Glu1988Lys
NM_000132.3:c.5962G>A NP_000123.1:p.Glu1988Lys
XM_011531126.1:c.5857G>A XP_011529428.1:p.Glu1953Lys
NM_000132.4:c.5962G>A MANE Select NP_000123.1:p.Glu1988Lys