Canonical Allele Identifier: CA2466845311
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154956985T= , CM000685.2:g.154956985T= GRCh38
NC_000023.10:g.154185260T= , CM000685.1:g.154185260T= GRCh37
NC_000023.9:g.153838454T= NCBI36
NG_011403.1:g.70739A=
NG_011403.2:g.70739A=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1724A= MANE Select ENSP00000353393.4:p.Lys575=
ENST00000647125.1:c.*1600A= ENSP00000496062.1:n.*1600A=
ENST00000360256.8:c.1724A= ENSP00000353393.4:p.Lys575=
NM_000132.3:c.1724A= NP_000123.1:p.Lys575=
XM_011531126.1:c.1619A= XP_011529428.1:p.Lys540=
NM_000132.4:c.1724A= MANE Select NP_000123.1:p.Lys575=