Canonical Allele Identifier: CA519371913
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154221224T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154992949T>C , CM000685.2:g.154992949T>C GRCh38
NC_000023.10:g.154221224T>C , CM000685.1:g.154221224T>C GRCh37
NC_000023.9:g.153874418T>C NCBI36
NG_011403.1:g.34775A>G
NG_011403.2:g.34775A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.588A>G MANE Select ENSP00000353393.4:p.Leu196=
ENST00000647125.1:c.*374A>G ENSP00000496062.1:n.*374A>G
ENST00000360256.8:c.588A>G ENSP00000353393.4:p.Leu196=
ENST00000423959.5:c.483A>G ENSP00000409446.1:p.Leu161=
NM_000132.3:c.588A>G NP_000123.1:p.Leu196=
XM_011531126.1:c.483A>G XP_011529428.1:p.Leu161=
NM_000132.4:c.588A>G MANE Select NP_000123.1:p.Leu196=