Canonical Allele Identifier: CA519363267
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154194263T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154965988T>C , CM000685.2:g.154965988T>C GRCh38
NC_000023.10:g.154194263T>C , CM000685.1:g.154194263T>C GRCh37
NC_000023.9:g.153847457T>C NCBI36
NG_011403.1:g.61736A>G
NG_011403.2:g.61736A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1425A>G MANE Select ENSP00000353393.4:p.Glu475=
ENST00000647125.1:c.*1301A>G ENSP00000496062.1:n.*1301A>G
ENST00000360256.8:c.1425A>G ENSP00000353393.4:p.Glu475=
ENST00000483822.2:n.245A>G
NM_000132.3:c.1425A>G NP_000123.1:p.Glu475=
XM_011531126.1:c.1320A>G XP_011529428.1:p.Glu440=
NM_000132.4:c.1425A>G MANE Select NP_000123.1:p.Glu475=