Canonical Allele Identifier: CA414916677
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154194845A>T (hg19) chrX:g.154966570A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154966570A>T , CM000685.2:g.154966570A>T GRCh38
NC_000023.10:g.154194845A>T , CM000685.1:g.154194845A>T GRCh37
NC_000023.9:g.153848039A>T NCBI36
NG_011403.1:g.61154T>A
NG_011403.2:g.61154T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1127T>A MANE Select ENSP00000353393.4:p.Val376Glu
ENST00000647125.1:c.*1003T>A ENSP00000496062.1:n.*1003T>A
ENST00000360256.8:c.1127T>A ENSP00000353393.4:p.Val376Glu
NM_000132.3:c.1127T>A NP_000123.1:p.Val376Glu
XM_011531126.1:c.1022T>A XP_011529428.1:p.Val341Glu
NM_000132.4:c.1127T>A MANE Select NP_000123.1:p.Val376Glu
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