Canonical Allele Identifier: CA2466835855
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928926C= , CM000685.2:g.154928926C= GRCh38
NC_000023.10:g.154157201C= , CM000685.1:g.154157201C= GRCh37
NC_000023.9:g.153810395C= NCBI36
NG_011403.1:g.98798G=
NG_011403.2:g.98798G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.4864G= MANE Select ENSP00000353393.4:p.Ala1622=
ENST00000360256.8:c.4864G= ENSP00000353393.4:p.Ala1622=
NM_000132.3:c.4864G= NP_000123.1:p.Ala1622=
XM_011531126.1:c.4759G= XP_011529428.1:p.Ala1587=
NM_000132.4:c.4864G= MANE Select NP_000123.1:p.Ala1622=