Canonical Allele Identifier: CA414910445
Gene: F8 HGNC NCBI

Linked Data

COSMIC: COSM4406830 COSM4406831
MyVariant Identifiers: chrX:g.154182191A>T (hg19) chrX:g.154953916A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154953916A>T , CM000685.2:g.154953916A>T GRCh38
NC_000023.10:g.154182191A>T , CM000685.1:g.154182191A>T GRCh37
NC_000023.9:g.153835385A>T NCBI36
NG_011403.1:g.73808T>A
NG_011403.2:g.73808T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.1879T>A MANE Select ENSP00000353393.4:p.Phe627Ile
ENST00000647125.1:c.*1755T>A ENSP00000496062.1:n.*1755T>A
ENST00000360256.8:c.1879T>A ENSP00000353393.4:p.Phe627Ile
NM_000132.3:c.1879T>A NP_000123.1:p.Phe627Ile
XM_011531126.1:c.1774T>A XP_011529428.1:p.Phe592Ile
NM_000132.4:c.1879T>A MANE Select NP_000123.1:p.Phe627Ile
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