Canonical Allele Identifier: CA414918209
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154197763T>A (hg19) chrX:g.154969488T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154969488T>A , CM000685.2:g.154969488T>A GRCh38
NC_000023.10:g.154197763T>A , CM000685.1:g.154197763T>A GRCh37
NC_000023.9:g.153850957T>A NCBI36
NG_011403.1:g.58236A>T
NG_011403.2:g.58236A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.852A>T MANE Select ENSP00000353393.4:p.Glu284Asp
ENST00000647125.1:c.*728A>T ENSP00000496062.1:n.*728A>T
ENST00000360256.8:c.852A>T ENSP00000353393.4:p.Glu284Asp
NM_000132.3:c.852A>T NP_000123.1:p.Glu284Asp
XM_011531126.1:c.747A>T XP_011529428.1:p.Glu249Asp
NM_000132.4:c.852A>T MANE Select NP_000123.1:p.Glu284Asp
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