Canonical Allele Identifier: CA414914488
Gene: F8 HGNC NCBI

Linked Data

COSMIC: COSM457142 COSM457143
MyVariant Identifiers: chrX:g.154194287G>C (hg19) chrX:g.154966012G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154966012G>C , CM000685.2:g.154966012G>C GRCh38
NC_000023.10:g.154194287G>C , CM000685.1:g.154194287G>C GRCh37
NC_000023.9:g.153847481G>C NCBI36
NG_011403.1:g.61712C>G
NG_011403.2:g.61712C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.1401C>G MANE Select ENSP00000353393.4:p.Ile467Met
ENST00000647125.1:c.*1277C>G ENSP00000496062.1:n.*1277C>G
ENST00000360256.8:c.1401C>G ENSP00000353393.4:p.Ile467Met
ENST00000483822.2:n.221C>G
NM_000132.3:c.1401C>G NP_000123.1:p.Ile467Met
XM_011531126.1:c.1296C>G XP_011529428.1:p.Ile432Met
NM_000132.4:c.1401C>G MANE Select NP_000123.1:p.Ile467Met
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