Canonical Allele Identifier: CA2466845308
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154956979G= , CM000685.2:g.154956979G= GRCh38
NC_000023.10:g.154185254G= , CM000685.1:g.154185254G= GRCh37
NC_000023.9:g.153838448G= NCBI36
NG_011403.1:g.70745C=
NG_011403.2:g.70745C=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1730C= MANE Select ENSP00000353393.4:p.Ser577=
ENST00000647125.1:c.*1606C= ENSP00000496062.1:n.*1606C=
ENST00000360256.8:c.1730C= ENSP00000353393.4:p.Ser577=
NM_000132.3:c.1730C= NP_000123.1:p.Ser577=
XM_011531126.1:c.1625C= XP_011529428.1:p.Ser542=
NM_000132.4:c.1730C= MANE Select NP_000123.1:p.Ser577=