Canonical Allele Identifier: CA519718439
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154157058T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928783T>A , CM000685.2:g.154928783T>A GRCh38
NC_000023.10:g.154157058T>A , CM000685.1:g.154157058T>A GRCh37
NC_000023.9:g.153810252T>A NCBI36
NG_011403.1:g.98941A>T
NG_011403.2:g.98941A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5007A>T MANE Select ENSP00000353393.4:p.Ile1669=
ENST00000360256.8:c.5007A>T ENSP00000353393.4:p.Ile1669=
NM_000132.3:c.5007A>T NP_000123.1:p.Ile1669=
XM_011531126.1:c.4902A>T XP_011529428.1:p.Ile1634=
NM_000132.4:c.5007A>T MANE Select NP_000123.1:p.Ile1669=
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