Canonical Allele Identifier: CA519384097
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154225258T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154996983T>C , CM000685.2:g.154996983T>C GRCh38
NC_000023.10:g.154225258T>C , CM000685.1:g.154225258T>C GRCh37
NC_000023.9:g.153878452T>C NCBI36
NG_011403.1:g.30741A>G
NG_011403.2:g.30741A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.378A>G MANE Select ENSP00000353393.4:p.Lys126=
ENST00000647125.1:c.*164A>G ENSP00000496062.1:n.*164A>G
ENST00000360256.8:c.378A>G ENSP00000353393.4:p.Lys126=
ENST00000423959.5:c.273A>G ENSP00000409446.1:p.Lys91=
ENST00000453950.1:c.360A>G ENSP00000389153.1:p.Lys120=
NM_000132.3:c.378A>G NP_000123.1:p.Lys126=
XM_011531126.1:c.273A>G XP_011529428.1:p.Lys91=
NM_000132.4:c.378A>G MANE Select NP_000123.1:p.Lys126=
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