Canonical Allele Identifier: CA2466828197
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904087T= , CM000685.2:g.154904087T= GRCh38
NC_000023.10:g.154132362T= , CM000685.1:g.154132362T= GRCh37
NC_000023.9:g.153785556T= NCBI36
NG_011403.1:g.123637A=
NG_011403.2:g.123637A=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5817A= MANE Select ENSP00000353393.4:p.Ala1939=
ENST00000360256.8:c.5817A= ENSP00000353393.4:p.Ala1939=
NM_000132.3:c.5817A= NP_000123.1:p.Ala1939=
XM_011531126.1:c.5712A= XP_011529428.1:p.Ala1904=
NM_000132.4:c.5817A= MANE Select NP_000123.1:p.Ala1939=