Canonical Allele Identifier: CA2466828198
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904088G= , CM000685.2:g.154904088G= GRCh38
NC_000023.10:g.154132363G= , CM000685.1:g.154132363G= GRCh37
NC_000023.9:g.153785557G= NCBI36
NG_011403.1:g.123636C=
NG_011403.2:g.123636C=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5816C= MANE Select ENSP00000353393.4:p.Ala1939=
ENST00000360256.8:c.5816C= ENSP00000353393.4:p.Ala1939=
NM_000132.3:c.5816C= NP_000123.1:p.Ala1939=
XM_011531126.1:c.5711C= XP_011529428.1:p.Ala1904=
NM_000132.4:c.5816C= MANE Select NP_000123.1:p.Ala1939=