Canonical Allele Identifier: CA519372730
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154221332C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154993057C>G , CM000685.2:g.154993057C>G GRCh38
NC_000023.10:g.154221332C>G , CM000685.1:g.154221332C>G GRCh37
NC_000023.9:g.153874526C>G NCBI36
NG_011403.1:g.34667G>C
NG_011403.2:g.34667G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.480G>C MANE Select ENSP00000353393.4:p.Leu160=
ENST00000647125.1:c.*266G>C ENSP00000496062.1:n.*266G>C
ENST00000360256.8:c.480G>C ENSP00000353393.4:p.Leu160=
ENST00000423959.5:c.375G>C ENSP00000409446.1:p.Leu125=
ENST00000453950.1:c.462G>C ENSP00000389153.1:p.Leu154=
NM_000132.3:c.480G>C NP_000123.1:p.Leu160=
XM_011531126.1:c.375G>C XP_011529428.1:p.Leu125=
NM_000132.4:c.480G>C MANE Select NP_000123.1:p.Leu160=
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