Canonical Allele Identifier: CA2466835853
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928923A= , CM000685.2:g.154928923A= GRCh38
NC_000023.10:g.154157198A= , CM000685.1:g.154157198A= GRCh37
NC_000023.9:g.153810392A= NCBI36
NG_011403.1:g.98801T=
NG_011403.2:g.98801T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.4867T= MANE Select ENSP00000353393.4:p.Cys1623=
ENST00000360256.8:c.4867T= ENSP00000353393.4:p.Cys1623=
NM_000132.3:c.4867T= NP_000123.1:p.Cys1623=
XM_011531126.1:c.4762T= XP_011529428.1:p.Cys1588=
NM_000132.4:c.4867T= MANE Select NP_000123.1:p.Cys1623=