Canonical Allele Identifier: CA519363884
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154194368C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154966093C>T , CM000685.2:g.154966093C>T GRCh38
NC_000023.10:g.154194368C>T , CM000685.1:g.154194368C>T GRCh37
NC_000023.9:g.153847562C>T NCBI36
NG_011403.1:g.61631G>A
NG_011403.2:g.61631G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.1320G>A MANE Select ENSP00000353393.4:p.Arg440=
ENST00000647125.1:c.*1196G>A ENSP00000496062.1:n.*1196G>A
ENST00000360256.8:c.1320G>A ENSP00000353393.4:p.Arg440=
ENST00000483822.2:n.140G>A
NM_000132.3:c.1320G>A NP_000123.1:p.Arg440=
XM_011531126.1:c.1215G>A XP_011529428.1:p.Arg405=
NM_000132.4:c.1320G>A MANE Select NP_000123.1:p.Arg440=