Canonical Allele Identifier: CA519719910
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154159728T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154931453T>C , CM000685.2:g.154931453T>C GRCh38
NC_000023.10:g.154159728T>C , CM000685.1:g.154159728T>C GRCh37
NC_000023.9:g.153812922T>C NCBI36
NG_011403.1:g.96271A>G
NG_011403.2:g.96271A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.2337A>G MANE Select ENSP00000353393.4:p.Thr779=
ENST00000647125.1:c.*2003A>G ENSP00000496062.1:n.*2003A>G
ENST00000360256.8:c.2337A>G ENSP00000353393.4:p.Thr779=
NM_000132.3:c.2337A>G NP_000123.1:p.Thr779=
XM_011531126.1:c.2232A>G XP_011529428.1:p.Thr744=
NM_000132.4:c.2337A>G MANE Select NP_000123.1:p.Thr779=
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